Pre-malignant signs of gastric MALT lymphoma

ABSTRACT

Mucosa-associated lymphoid tissue (MALT) lymphoma is the most common type of extra-nodal non-Hodgkin lymphoma, which mostly involves the stomach. The clinical suspicion and diagnosis are often challenging because of the lack of specific symptoms and conventional endoscopic findings. Three magnifying endoscopic signs of the gastric mucosa have been described as highly specific to the diagnosis of MALT lymphoma, such as (i) tree-like appearance of the microvessels; (ii) non-structural area; and (iii) ballooning crypt pattern. We report the case of a middle-aged woman in which these signs appeared chronologically over a period of 2 years, showing the association of the sequence of the endoscopic findings and the final histological diagnosis of gastric MALT lymphoma.

Keywords
Lymphoma; B-Cell; Marginal Zone; Endoscopy

INTRODUCTION

MALT lymphoma is the most common type of extra-nodal non-Hodgkin lymphoma that mostly involves the stomach.^1,2 The clinical suspicion is virtually absent, based on the symptoms, and the diagnosis is often challenging because of the non-specificity of the conventional endoscopic findings.

Patients with gastric MALT lymphoma can be asymptomatic or can present vague dyspeptic complaints. With conventional white light endoscopy, the mucosal alterations can mimic gastric lesions of different entities, such as gastritis, peptic ulcer, polyps, early or advanced gastric cancer, and subepithelial lesions.^3-5

The growing use of high-magnification endoscopes and the enhancement of computed virtual chromoendoscopy are improving the early endoscopic diagnosis of many gastrointestinal diseases. These new techniques have increased the effectiveness of the diagnosis and have been changing the course and management of many entities.^6-11

Ono et al.^12,13 and Nonaka et al.¹⁴ described new signs of gastric MALT lymphoma; namely (i) the complete disappearance of the gastric mucosa’s microstructure; and (ii) the tree-like appearance of dilated vessels, both identified on magnified virtual chromoendoscopy. Recent studies^4,13,14 endorsed the high sensitivity and specificity of these alterations and showed the usefulness of post-treatment endoscopic follow-up. Another sign of gastric MALT lymphoma is crypt swelling, which is also called “ballooning” (Figures 11B).¹³

Figure 1
Endoscopic images. A – Yellow traced line: non-structural area with tortuous vessels; red arrow: ballooning crypt pattern. B – The white arrow points to tree-like dilated vessels inside a non-structural area. The surrounding mucosa presents a ballooning crypt pattern. C – Red flat lesion on the great curvature of the antrum. D – Indigo-carmine staining of the antral lesion.

We present a case in which the ballooning crypt pattern (BCP) and an area with microstructure loss and tortuous vessels were observed on the initial endoscopic assessment of a middle-aged woman. Although no malignancy was detected on the first target biopsy specimens, the development of tree-like dilated vessels and an increase in the size of the area with a loss of microstructure was observed over a period of 2 years. With these new findings MALT lymphoma was confirmed by the histopathologic examination.

CASE REPORT

A 41-year-old female patient, previously diagnosed with Sjögren syndrome, and with a family history of gastric adenocarcinoma (her mother was diagnosed at the age of 65 years), was submitted to an upper gastrointestinal (UGI) endoscopy for gastric cancer screening. The gastric mucosa presented signs of chronic gastritis without atrophy, and a flat red area at the great curvature of the proximal antrum was depicted (Figure 1C). The indigo carmine staining was performed, and showed a discrete granulation of the mucosa (Figure 1D).

In a close-up view, a marked swelling of the crypts (ballooning) was detected within the lesion (Figures 2A). A thorough examination of this area detected a 2 mm depression, which presented a complete loss of the microstructure and was accompanied by tortuous vessels; however, there was no dilation or tree-like arrangement (Figure 2B).

Figure 2
Endoscopic images. A – Close up view of the lesion with indigo-carmine staining without magnification. B – Magnified view of the lesion with FICE (virtual chromoendoscopy) showing a small depressed non-structural area (2 mm) with tortuous vessels within the lesion. FICE = Fuji Intelligent Color Enhancement.

These findings raised the suspicion of an early adenocarcinoma (0-IIb presentation), and target biopsies were sampled (Figure 3).

Figure 3
Endoscopic image showing a close-up view of the lesion with indigo-carmine staining without magnification, in which the ballooning crypt pattern can be observed, and the guided biopsy site.

The histopathologic analyses showed plasmacytic proliferation at the lamina propria and rare lymphoepithelial cluster lesions. However, the immunohistochemistry (IHC) was not consistent with the diagnosis of MALT lymphoma.

An endoscopy with biopsies was repeated 3 months later with the same results, and was scheduled annually thereafter.

One year after the first examination, the patient's antral gastric mucosa presented signs of atrophy, and the size of the flattened red area remained steady; however, the diameter of the non-structural area was slightly enlarged. The vessels’ gauge and the tortuous shape were kept unchanged, as was the BCP and the histologic examination.

After 2 years of follow-up, and with four UGI endoscopies performed, we identified tree-like dilated vessels, an enlargement of the non-structural area size, and the maintenance of the BCP (Figures 11B). At this time, the biopsy revealed dense lymphoid infiltrate with plasmacytic features in the lamina propria mucosa, with occasional lymphoepithelial lesions, and displaced gastric glands (Figure 4), raising the hypothesis of MALT lymphoma of a plasmacytic type.

Figure 4
Photomicrograph of the gastric biopsy; dense lymphoplasmacytic infiltrate expanding lamina propria, and displacing gastric glands. Note the focal lymphoepithelial lesion (H&E, 400X).

The IHC study demonstrated positivity for CD79a, CD43, and CD138, and negativity for CD20, CD5, CD23, and CD10 (Figures 5 A-D and 66B). Additionally, there was a clear restriction for immunoglobulin light chain lambda, which was strong and diffusely positive in neoplastic cells. Kappa light chains were positive in rare reactive plasma cells (Figures 66D).

Figure 5
Photomicrograph of the gastric biopsy showing immunohistochemistry panel results. A – Diffuse positivity for CD79a (400X). B – Diffuse positivity for CD138 (400X). C – Diffuse positivity for CD43 (400X). D – CD10 negative (200X).

Figure 6
Photomicrograph of the gastric biopsy showing immunohistochemistry panel results. A – Negative for CD5 (200X). B – Negative for CD23 (100X). C – Strong and diffuse positivity for lambda light (200X). D – Rare cells positive for kappa light chain (400X).

The histological and IHC analysis rendered the diagnosis of an extranodal marginal zone lymphoma with marked plasmacytic differentiation.

According to the European Society of Medical Oncology guidelines for gastric MALT lymphoma,¹⁵ the patient was diagnosed as stage I using the Lugano staging system, which means she had a superficial lesion restricted to the gastrointestinal tract.

Helicobacter pylori infection was present in the first gastric biopsy, and eradication was confirmed 3 months later by histology. However, H. pylori infection was detected once again in histological analysis after 2 years. New eradication therapy was conducted and confirmed by urea breath test.

The patient was followed-up every 3-months with UGI endoscopy with biopsies; to date there has not been a complete remission of the lymphoma. During this period, fluorescence in situ hybridization (FISH) was performed, with a negative result for t(11;18) chromosomal translocation. If complete remission is not achieved within 1 year from the negative urea breath test, combined radiotherapy and chemotherapy is scheduled.

DISCUSSION

We present a case of gastric MALT lymphoma in its earliest original lesion observing the relationship between the magnifying endoscopic findings with the histology in a chronological assessment.

Wotherspoon’s grading system score for MALT lymphoma considers the presence of marginal zone cells and prominent lymphoepithelial lesions infiltrating the lamina propria as the key findings for the diagnosis.¹⁶ In the presented case, these alterations were only found after 2 years of follow-up, when the enlargement of the non-structural area and the emergence of dilated tree-like vessels were depicted. Even the IHC could not confirm the MALT lymphoma diagnosis before the microvascular and microstructural changes.

The study by Ono et al.¹³ shows 100% specificity for BCP in confirmed cases of gastric MALT lymphoma. Indeed, in our case, the BCP was present from the very first exam; however, it was not associated with the histological and IHC diagnosis of MALT lymphoma. This mucosal structural change-as an isolated finding-did not correlate with the lymphoepithelial infiltration of the gastric mucosa nor with the typical IHC panel. We observed the appearance of the magnifying endoscopic signs chronologically in this case. BCP seemed to precede the malignancy, as did small foci of non-structural areas (< 5 mm). Dense infiltration of the lymphoepithelial lesions was only observed after the expansion of the non-structural areas and the appearance of the tree-like dilated vessels.

Therefore, the histopathologic examination may not identify signs of malignancy on target biopsies of BCP and of non-structural areas smaller than 5 mm. Thus, we propose that these might be considered pre-malignant signs of gastric MALT lymphoma.

• How to cite: Hassegawa RT, Ogawa EKM, Ibrahim RE, Venco FE, Maruta LM. Pre-malignant signs of gastric MALT lymphoma. Autops Case Rep [Internet]. 2020;10(1): e2019130. https://doi.org/10.4322/acr.2019.130
• The authors retain an informed consent signed by the patient authorizing publication of the data.
• Financial support: None

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Publication Dates

• Publication in this collection
  21 Oct 2020
• Date of issue
  2020

History

• Received
  01 Nov 2018
• Accepted
  16 Sept 2019