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Unveiling an oral hemangiolymphangioma

ABSTRACT

Hemangiolymphangioma is a very rare vascular malformation that develops as a combination of dilated venous and lymphatic vessels. We describe an unusual case of hemangiolymphangioma of the tongue affecting an adult man who complained of an uncomfortable, slowly progressing exophytic irregular dark red-violaceous nodular mass on his tongue that impaired speech and swallowing for two weeks. The clinical differential diagnoses were Kaposi’s sarcoma and a COVID-19-related lesion. A complete blood count and serology for HIV-1 and 2 and RT-PCR for COVID-19 were requested and results were negative. An incisional biopsy was performed. Microscopically, the lesion exhibited several dilated vessels lined by normal-appearing endothelial cells, some filled with prominent intravascular erythrocytes and others containing proteinaceous eosinophilic material resembling lymphatic vessels, in close association with hyperkeratosis, papillomatosis, and acanthosis. From immunohistochemical analysis, most vessels were found to be CD34 positive, some highlighted by α-SMA, whereas D2-40 was focal. Positive staining for some lymphatic and blood vessel markers, i.e., D2-40 and CD34, respectively, indicates a mixed derivation of the lesion. HHV-8 was negative. Clinical features, the congested blood vessels with ectasia in intimate association with hyperplastic epithelium, and the immunohistochemical profile supported the final diagnosis of oral hemangiolymphangioma. The patient underwent minimally invasive surgical excision with no intercurrences. After 18 months of follow-up, there were no signs of relapse.

Keywords
Angiokeratoma; lymphangioma; COVID-19; tongue; case reports

INTRODUCTION

Hemangiolymphangioma is a very rare vascular malformation.11 Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.

2 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
-33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
In vascular tumors, blood vessel architecture is incomplete and surrounded by hyperplastic cells.44 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...
,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5. On the other hand, vascular malformations consist of progressively enlarging ectatic vessels composed of veins, lymphatic vessels, venules, capillaries, arteries, or mixed vessel types.44 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...
,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5. Histologically, different combinations of vascular elements, such as lymphatic and venous endothelium, may be seen in the same lesion,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,44 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...
and these vascular spaces may be filled with red blood cells and proteinaceous fluid similar to lymph fluid.33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5. These mixed vascular malformations are termed ‘hemangiolymphangioma’ or ‘lymphangiohemangioma’ according to the prevalent vessel structure.33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...

Clinically, hemangiolymphangiomas may be diagnosed as red-to-violaceous plaques, papules, or nodules.33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,44 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...
,66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.

7 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
-88 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...
Tongue lesions may increase in size resulting in macroglossia, which can lead to breathing, mastication, deglutition, and speech dysfunction.66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.,88 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...
,99 Shetty DC, Urs AB, Rai HC, Ahuja N, Manchanda A. Case series on vascular malformation and their review with regard to terminology and categorization. Contemp Clin Dent. 2010;1(4):259-62. http://dx.doi.org/10.4103/0976-237X.76397. PMid:22114434.
http://dx.doi.org/10.4103/0976-237X.7639...
Oral lesions may resemble hemangioma,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
lymphangioma,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...
angiokeratoma,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
pyogenic granulomas,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...
Kaposi’s sarcoma,1212 Huang AY, Lin CL, Chen GS, Hu SC. Clinical features of Kaposi’s sarcoma: experience from a Taiwanese medical center. Int J Dermatol. 2019;58(12):1388-97. http://dx.doi.org/10.1111/ijd.14476. PMid:31102268.
http://dx.doi.org/10.1111/ijd.14476...
and purple vesiculobullous lesions and nodules as in COVID-19 patients.1313 Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: a review article. Dermatol Ther. 2021;34(1):e14578. http://dx.doi.org/10.1111/dth.14578. PMid:33236823.
http://dx.doi.org/10.1111/dth.14578...

Microscopically, hemangiolymphangiomas, like other vascular malformations, do not show active cellular proliferation,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
but appear as subepithelial enlarged channels (veins, capillaries, arteries, and lymphatic vessels).22 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
Just beneath the stratified squamous epithelium with elongation of rete ridges, there are multiple dilated vessels lined by normal-appearing endothelial cells.11 Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5. Vessels are capable of accumulating fluids. In hemangiolymphangiomas, most vascular channels contain erythrocytes, with or without thrombi formation, partly or completely enclosed by papillomatous epithelial tissue.11 Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.,66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91. Inflammatory components are not observed in the specimens.55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...
The definite diagnosis of hemangiolymphangioma may require investigation of clinical, microscopic, and immunohistochemical features.66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1414 Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729.
http://dx.doi.org/10.5272/jimab.2019254....
,1515 Wang L, Yuan W, Geng S, et al. Expression of lymphatic markers in angiokeratomas. J Cutan Pathol. 2014;41(7):576-81. http://dx.doi.org/10.1111/cup.12349. PMid:24666194.
http://dx.doi.org/10.1111/cup.12349...
In addition, clinicians must search for familial medical history and assess the results of laboratory tests to exclude genetic alterations, HIV infection, as well as COVID-19 with its systemic and oral involvement.33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
,99 Shetty DC, Urs AB, Rai HC, Ahuja N, Manchanda A. Case series on vascular malformation and their review with regard to terminology and categorization. Contemp Clin Dent. 2010;1(4):259-62. http://dx.doi.org/10.4103/0976-237X.76397. PMid:22114434.
http://dx.doi.org/10.4103/0976-237X.7639...
,1212 Huang AY, Lin CL, Chen GS, Hu SC. Clinical features of Kaposi’s sarcoma: experience from a Taiwanese medical center. Int J Dermatol. 2019;58(12):1388-97. http://dx.doi.org/10.1111/ijd.14476. PMid:31102268.
http://dx.doi.org/10.1111/ijd.14476...
,1313 Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: a review article. Dermatol Ther. 2021;34(1):e14578. http://dx.doi.org/10.1111/dth.14578. PMid:33236823.
http://dx.doi.org/10.1111/dth.14578...
Remarkably, the tongue appears to be a frequent site for COVID-19-related oral manifestations.1313 Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: a review article. Dermatol Ther. 2021;34(1):e14578. http://dx.doi.org/10.1111/dth.14578. PMid:33236823.
http://dx.doi.org/10.1111/dth.14578...

In contrast to hemangiomas, spontaneous regression of hemangiolymphangiomas is rarely observed.55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,1414 Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729.
http://dx.doi.org/10.5272/jimab.2019254....
Various therapeutic approaches have been proposed based on the size, type, and location of a lesion, as well as its association with anatomic structures and infiltration to the surrounding tissues.44 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...
,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,77 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...
,88 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...
,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...
,1414 Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729.
http://dx.doi.org/10.5272/jimab.2019254....
,1616 Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024. PMid:15635551.
http://dx.doi.org/10.1016/j.joms.2004.04...
Nevertheless, complete surgical excision is still the usual treatment option for these lesions whenever possible.55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...

This clinical case report comprises a survey of published cases and adds information to the scant literature on oral hemangiolymphangiomas.

CASE REPORT

A 23-year-old man attended a private clinic complaining of an uncomfortable, slowly progressing mass on his tongue that impaired speech and swallowing and had been present for two weeks. During anamnesis, he mentioned that he used to smoke Cannabis sativa. He did not indicate comorbidities. He denied having a cough, runny nose, nasal congestion, or fever. The intraoral examination revealed a painless exophytic irregular dark red-violaceous nodular lesion in the tongue’s right ventral and lateral border and a similar papule in the ipsilateral dorsal region surrounded by white plaques (Figure 1A).

Figure 1
Preoperative vs postoperative clinical features and microscopic analyses: A - Clinical aspect of an exophytic irregular yellowish and dark red-violaceous nodular lesion in right ventral and lateral border of the tongue; B - After 18 months of follow-up, no recurrence was noticed; C - Photomicrograph showing squamous epithelium with acanthosis, hyperparakeratosis, and elongated rete ridges, which encompassed dilated and congested vessels. (H&E, 10X); D - Photomicrograph presenting vascular spaces delimited by normal-appearing endothelial cells containing inside numerous erythrocytes and proteinaceous eosinophilic material. (H&E, 10X).

Under the clinical hypotheses of Kaposi’s sarcoma (KS) and COVID-19-related lesions, an incisional biopsy was performed. And a complete blood count and serology for Human Immunodeficiency Virus (HIV) 1 and 2, as well as a SARS-CoV-2 reverse-transcriptase-polymerase-chain-reaction test (RT-PCR test for COVID-19) were requested. Nasopharyngeal and oropharyngeal swabs were taken for RT-PCR test. None of the examinations showed abnormalities.

Microscopically, hyperparakeratosis, acanthosis, and papillomatosis in close association with large, dilated vessels lined by normal-appearing endothelial cells and containing inside erythrocytes and proteinaceous eosinophilic material were observed (Figure 1C-D).

An immunohistochemical panel was performed. Most vessels were CD34 positive; some were highlighted by α-SMA, whereas D2-40 was focal (Figure 2A-C). Human Herpes Virus 8 (HHV-8) was negative.

Figure 2
Immunohistochemical reactions. A - Most vessels showing positivity for CD34; B - Some vessels were highlighted by α-SMA; C - Focal positivity for D2-40. (DAB stain, 10X).

Based on the clinical, microscopical, and immunohistochemical features, a definitive diagnosis of hemangiolymphangioma was obtained. The patient underwent minimally invasive surgical excision. After 18 months of follow-up, there were no signs of relapse (Figure 1B).

An electronic search was conducted in PubMed, Scopus, and Web of Science for studies published up to August 2022, with the following keywords: (“hemangiolymphangioma” OR “lymphangiohemangioma”) AND (“oral lesions” OR “mucosal lesions”). Related articles were also searched in the reference lists of the found full-text articles. 16 full-text articles were evaluated,33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1212 Huang AY, Lin CL, Chen GS, Hu SC. Clinical features of Kaposi’s sarcoma: experience from a Taiwanese medical center. Int J Dermatol. 2019;58(12):1388-97. http://dx.doi.org/10.1111/ijd.14476. PMid:31102268.
http://dx.doi.org/10.1111/ijd.14476...
,1616 Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024. PMid:15635551.
http://dx.doi.org/10.1016/j.joms.2004.04...

17 Kim SS. Intraosseous hemangiolymphangioma of the mandible: a case report. J Korean Assoc Oral Maxillofac Surg. 2003;29(3):182-5.

18 Hunchaisri N. Hemangiolymphangioma of the floor of mouth: a case report and literature review. J Med Health Sci. 2013;20(3):4-9.

19 Duque CS, Londoño AF, Penagos AM, Urquijo DP, Dueñas JP. Hypoglossal nerve monitoring, a potential application of intraoperative nerve monitoring in head and neck surgery. World J Surg Oncol. 2013;11:225. http://dx.doi.org/10.1186/1477-7819-11-225. PMid:24028712.
http://dx.doi.org/10.1186/1477-7819-11-2...
-2020 Gautam D, Pantha T. Lymphamgiohemangioma of face: case report. Nepalese J ENT Head Neck Surg. 2020;11(2):28-30. of which two were excluded because the lesions were in the parotid gland and neck, respectively. Table 1 summarizes cases reported in scientific journals. Eight were located on the tongue,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.,88 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...
,99 Shetty DC, Urs AB, Rai HC, Ahuja N, Manchanda A. Case series on vascular malformation and their review with regard to terminology and categorization. Contemp Clin Dent. 2010;1(4):259-62. http://dx.doi.org/10.4103/0976-237X.76397. PMid:22114434.
http://dx.doi.org/10.4103/0976-237X.7639...
,1616 Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024. PMid:15635551.
http://dx.doi.org/10.1016/j.joms.2004.04...
,1919 Duque CS, Londoño AF, Penagos AM, Urquijo DP, Dueñas JP. Hypoglossal nerve monitoring, a potential application of intraoperative nerve monitoring in head and neck surgery. World J Surg Oncol. 2013;11:225. http://dx.doi.org/10.1186/1477-7819-11-225. PMid:24028712.
http://dx.doi.org/10.1186/1477-7819-11-2...
being 3 cases reported by Jian.1616 Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024. PMid:15635551.
http://dx.doi.org/10.1016/j.joms.2004.04...

Table 1
Published case reports33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...

4 Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534.
http://dx.doi.org/10.15406/jdhodt.2020.1...

5 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.

6 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.

7 Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379. PMid:23833496.
http://dx.doi.org/10.4103/0975-5950.1113...

8 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...

9 Shetty DC, Urs AB, Rai HC, Ahuja N, Manchanda A. Case series on vascular malformation and their review with regard to terminology and categorization. Contemp Clin Dent. 2010;1(4):259-62. http://dx.doi.org/10.4103/0976-237X.76397. PMid:22114434.
http://dx.doi.org/10.4103/0976-237X.7639...
-1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1212 Huang AY, Lin CL, Chen GS, Hu SC. Clinical features of Kaposi’s sarcoma: experience from a Taiwanese medical center. Int J Dermatol. 2019;58(12):1388-97. http://dx.doi.org/10.1111/ijd.14476. PMid:31102268.
http://dx.doi.org/10.1111/ijd.14476...
,1616 Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024. PMid:15635551.
http://dx.doi.org/10.1016/j.joms.2004.04...

17 Kim SS. Intraosseous hemangiolymphangioma of the mandible: a case report. J Korean Assoc Oral Maxillofac Surg. 2003;29(3):182-5.

18 Hunchaisri N. Hemangiolymphangioma of the floor of mouth: a case report and literature review. J Med Health Sci. 2013;20(3):4-9.

19 Duque CS, Londoño AF, Penagos AM, Urquijo DP, Dueñas JP. Hypoglossal nerve monitoring, a potential application of intraoperative nerve monitoring in head and neck surgery. World J Surg Oncol. 2013;11:225. http://dx.doi.org/10.1186/1477-7819-11-225. PMid:24028712.
http://dx.doi.org/10.1186/1477-7819-11-2...
-2020 Gautam D, Pantha T. Lymphamgiohemangioma of face: case report. Nepalese J ENT Head Neck Surg. 2020;11(2):28-30. on hemangiolymphangioma and lymphangiohemangioma of the oral cavity

DISCUSSION

Hemangiolymphangioma occurring exclusively in the oral cavity is very scarce11 Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.

2 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
-33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
as the most frequent sites are the neck’s anterior and posterior cervical triangle.22 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
Moreover, a histological assessment may be challenging because of its similarity with other vascular lesions, such as lymphangioma, and angiokeratoma.66 Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1414 Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729.
http://dx.doi.org/10.5272/jimab.2019254....
Lymphangioma has been suggested to be the lymphatic counterpart of angiokeratoma,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
,1515 Wang L, Yuan W, Geng S, et al. Expression of lymphatic markers in angiokeratomas. J Cutan Pathol. 2014;41(7):576-81. http://dx.doi.org/10.1111/cup.12349. PMid:24666194.
http://dx.doi.org/10.1111/cup.12349...
which demonstrates immunopositivity for CD31 and CD34.1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
Hemangiolymphangiomas are mixed lesions, and like angiokeratomas, may present positive staining for some lymphatic markers, i.e., CD31 and D2-40,22 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
which supports their lymphatic derivation. Consistent with previous reports,22 Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168. PMid:28928923.
http://dx.doi.org/10.1093/jscr/rjx168...
,1010 Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003. PMid:24491964.
http://dx.doi.org/10.1016/j.oooo.2013.12...
this specimen showed immunoreactivity for CD34 and focal positivity for D2-40.

In this case, it may be hypothesized that there were two etiopathogeneses. A vascular malformation may have developed from birth, although not apparent, and persisted until the patient noted the swelling.33 Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17. PMid:28932041.
http://dx.doi.org/10.4103/jomfp.JOMFP_28...
Conversely, the lesion could also be an acquired vascular malformation caused by mechanical trauma in an area with anomalous blood and lymphatic vessels.1414 Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729.
http://dx.doi.org/10.5272/jimab.2019254....
In hemangiolymphangiomas, the increased proliferative capacity of the stratified squamous epithelium seems to be a secondary reaction to vascular ectasia.2121 Sion-Vardy N, Manor E, Puterman M, Bodner L. Solitary angiokeratoma of the tongue. Med Oral Patol Oral Cir Bucal. 2008;13(1):E12-4. PMid:18167473. Acanthosis, elongated rete pegs, and hyperparakeratosis encase dilated vessels, which may contain red blood cells, thrombi, and eosinophilic proteinaceous material.11 Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.,55 Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.,88 Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x. PMid:2981911.
http://dx.doi.org/10.1111/j.1524-4725.19...
,1111 Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002.
http://dx.doi.org/10.1016/j.ajoms.2015.1...

After the physical clinical examination, based on its features, such as an exophytic irregular dark red-violaceous nodular lesion, the clinical hypothesis of KS and a COVID-19-related lesion was made. The latter was because of the COVID-19 outbreak, in 2020. Some authors published the COVID-19-related vascular alteration of the tongue,1313 Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: a review article. Dermatol Ther. 2021;34(1):e14578. http://dx.doi.org/10.1111/dth.14578. PMid:33236823.
http://dx.doi.org/10.1111/dth.14578...
similar to our report. KS is the most common neoplasm associated with HIV. In nearly 20% of patients, the initial manifestation of HIV infection is in the mouth. Therefore, we ruled out all these clinical hypotheses.

In a multicenter study of oral lymphatic malformations, disagreement between clinical and histopathological diagnoses was encountered in 58.2% of the lesions.2222 Meirelles DP, do Couto AM, Silva LVO, et al. Oral lymphatic malformations: a multicenter study of 208 cases and literature review. Head Neck. 2021;43(11):3562-71. http://dx.doi.org/10.1002/hed.26854. PMid:34517432.
http://dx.doi.org/10.1002/hed.26854...
Considering that vascular lesions within the mouth have a broad etiopathogenesis, the final diagnosis of such entities may be challenging.2323 Brahmbhatt AN, Skalski KA, Bhatt AA. Vascular lesions of the head and neck: an update on classification and imaging review. Insights Imaging. 2020;11(1):19. http://dx.doi.org/10.1186/s13244-019-0818-3. PMid:32034537.
http://dx.doi.org/10.1186/s13244-019-081...
To improve the diagnostic process and establish a definite diagnosis of an uncommon lesion, this study described the immunohistochemical profile of an oral hemangiolymphangioma.

A thorough evaluation of a vascular lesion was presented and the diagnosis of hemangiolymphangioma of the tongue was assessed by histopathological and immunohistochemical analysis. Well-documented cases of hemangiolymphangioma are important for further categorization of mixed vascular malformations.

  • How to cite: Ferreira-Santos RI, Santos KA, Scherma AP, León JE, Kaminagakura E. Unveiling an oral hemangiolymphangioma. Autops Case Rep [Internet]. 2023;13:e2023435. https://doi.org/10.4322/acr.2023.435
  • This study was carried out at São Paulo State University (UNESP), Department of Biosciences and Oral Diagnosis, São José dos Campos, São Paulo, Brazil.
  • Ethics statement: The procedures performed in studies involving human participants were in accordance with the ethical standards of the institution, the national research committee, and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The authors retain informed consent signed by the patient authorizing data publication.
  • Financial support: None

REFERENCES

  • 1
    Kulkarni CV, Nema P, Patidar H, Soni S, Tiwari NP. Hemangiolymphangioma of neck - a rare case with review report. J Med Sci Clin Res. 2014;2(8):1869-72.
  • 2
    Murphy T, Ramai D, Lai J, Sullivan K, Grimes C. Adult neck hemangiolymphangioma: a case and review of its etiology, diagnosis and management. J Surg Case Rep. 2017;2017(8):rjx168. http://dx.doi.org/10.1093/jscr/rjx168 PMid:28928923.
    » http://dx.doi.org/10.1093/jscr/rjx168
  • 3
    Manickam S, Sasikumar P, Kishore BN, Joy S. Hemangiolymphangioma of buccal mucosa: a rare case report. J Oral Maxillofac Pathol. 2017;21(2):282-5. http://dx.doi.org/10.4103/jomfp.JOMFP_28_17 PMid:28932041.
    » http://dx.doi.org/10.4103/jomfp.JOMFP_28_17
  • 4
    Khaunte DDN, Kumar PS, Dhupar V, Naik M. Hemangiolymphangioma of buccal cheek - a rare case report with review of literature. J Dent Health Oral Disord Ther. 2020;11(5):150-4. http://dx.doi.org/10.15406/jdhodt.2020.11.00534
    » http://dx.doi.org/10.15406/jdhodt.2020.11.00534
  • 5
    Shetty D, Rai H, Rastogi P, Panda A, Ahuja N. Vascular malformations of the oral cavity in children and young adolescents - insights into their pathogenesis. Internet J Ped Neonatol. 2009;12(2):1-5.
  • 6
    Merhi BA, Nous A, Rajab M. Hemangiolymphangioma of tongue, report of a rare case. Eur J Biomed Pharm Sci. 2016;3(5):88-91.
  • 7
    Sobhana CR, Beena VT, Soni A, Choudhary K, Sapru D. Hemangiolymphangioma of buccal mucosa: report of a rare case and review of literature on treatment aspect. Natl J Maxillofac Surg. 2012;3(2):190-4. http://dx.doi.org/10.4103/0975-5950.111379 PMid:23833496.
    » http://dx.doi.org/10.4103/0975-5950.111379
  • 8
    Vilalta J, Mascaro JM. Hemangiolymphangioma of the tongue treated by transfixion technique. J Dermatol Surg Oncol. 1985;11(2):168-70. http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x PMid:2981911.
    » http://dx.doi.org/10.1111/j.1524-4725.1985.tb02986.x
  • 9
    Shetty DC, Urs AB, Rai HC, Ahuja N, Manchanda A. Case series on vascular malformation and their review with regard to terminology and categorization. Contemp Clin Dent. 2010;1(4):259-62. http://dx.doi.org/10.4103/0976-237X.76397 PMid:22114434.
    » http://dx.doi.org/10.4103/0976-237X.76397
  • 10
    Katsoulas N, Tosios KI, Argyris P, Koutlas IG, Sklavounou A. Lymphangioma circumscriptum, angiokeratoma, or superficial vascular ectasia with epithelial hyperplasia? Oral Surg Oral Med Oral Pathol Oral Radiol. 2014;118(2):e53-7. http://dx.doi.org/10.1016/j.oooo.2013.12.003 PMid:24491964.
    » http://dx.doi.org/10.1016/j.oooo.2013.12.003
  • 11
    Yarmand F, Seyyedmajidi M, Shirzadc A, Foroughi R, Bakhshian A. Lymphangiohemangioma of buccal mucosa: report of a rare case. J Oral Maxillofac Surg Med Pathol. 2016;28(4):358-61. http://dx.doi.org/10.1016/j.ajoms.2015.11.002
    » http://dx.doi.org/10.1016/j.ajoms.2015.11.002
  • 12
    Huang AY, Lin CL, Chen GS, Hu SC. Clinical features of Kaposi’s sarcoma: experience from a Taiwanese medical center. Int J Dermatol. 2019;58(12):1388-97. http://dx.doi.org/10.1111/ijd.14476 PMid:31102268.
    » http://dx.doi.org/10.1111/ijd.14476
  • 13
    Iranmanesh B, Khalili M, Amiri R, Zartab H, Aflatoonian M. Oral manifestations of COVID-19 disease: a review article. Dermatol Ther. 2021;34(1):e14578. http://dx.doi.org/10.1111/dth.14578 PMid:33236823.
    » http://dx.doi.org/10.1111/dth.14578
  • 14
    Deliverska E. Hemangiolymphangioma of the mandible: case report. J IMAB. 2019;25(4):2729-32. http://dx.doi.org/10.5272/jimab.2019254.2729
    » http://dx.doi.org/10.5272/jimab.2019254.2729
  • 15
    Wang L, Yuan W, Geng S, et al. Expression of lymphatic markers in angiokeratomas. J Cutan Pathol. 2014;41(7):576-81. http://dx.doi.org/10.1111/cup.12349 PMid:24666194.
    » http://dx.doi.org/10.1111/cup.12349
  • 16
    Jian XC. Surgical management of lymphangiomatous or lymphangiohemangiomatous macroglossia. J Oral Maxillofac Surg. 2005;63(1):15-9. http://dx.doi.org/10.1016/j.joms.2004.04.024 PMid:15635551.
    » http://dx.doi.org/10.1016/j.joms.2004.04.024
  • 17
    Kim SS. Intraosseous hemangiolymphangioma of the mandible: a case report. J Korean Assoc Oral Maxillofac Surg. 2003;29(3):182-5.
  • 18
    Hunchaisri N. Hemangiolymphangioma of the floor of mouth: a case report and literature review. J Med Health Sci. 2013;20(3):4-9.
  • 19
    Duque CS, Londoño AF, Penagos AM, Urquijo DP, Dueñas JP. Hypoglossal nerve monitoring, a potential application of intraoperative nerve monitoring in head and neck surgery. World J Surg Oncol. 2013;11:225. http://dx.doi.org/10.1186/1477-7819-11-225 PMid:24028712.
    » http://dx.doi.org/10.1186/1477-7819-11-225
  • 20
    Gautam D, Pantha T. Lymphamgiohemangioma of face: case report. Nepalese J ENT Head Neck Surg. 2020;11(2):28-30.
  • 21
    Sion-Vardy N, Manor E, Puterman M, Bodner L. Solitary angiokeratoma of the tongue. Med Oral Patol Oral Cir Bucal. 2008;13(1):E12-4. PMid:18167473.
  • 22
    Meirelles DP, do Couto AM, Silva LVO, et al. Oral lymphatic malformations: a multicenter study of 208 cases and literature review. Head Neck. 2021;43(11):3562-71. http://dx.doi.org/10.1002/hed.26854 PMid:34517432.
    » http://dx.doi.org/10.1002/hed.26854
  • 23
    Brahmbhatt AN, Skalski KA, Bhatt AA. Vascular lesions of the head and neck: an update on classification and imaging review. Insights Imaging. 2020;11(1):19. http://dx.doi.org/10.1186/s13244-019-0818-3 PMid:32034537.
    » http://dx.doi.org/10.1186/s13244-019-0818-3

Publication Dates

  • Publication in this collection
    29 May 2023
  • Date of issue
    2023

History

  • Received
    21 Oct 2022
  • Accepted
    29 Apr 2023
Hospital Universitário da Universidade de São Paulo Hospital Universitário da Universidade de São Paulo, Av. Prof. Lineu Prestes, 2565 - Cidade Universitária, 05508-000 - São Paulo - SP - Brasil, (16) 3307-2068, (16) 3307-2068 - São Paulo - SP - Brazil
E-mail: autopsy.hu@gmail.com