Primary mucosa associated lymphoid tissue lymphoma of the gallbladder: A case report and review of literature.

in World journal of clinical cases by Mi-Rin Lee, Kyu-Yun Jang, Jae-Do Yang

TLDR

  • A rare case of primary MALT lymphoma of the gallbladder is reported in an 82-year-old man, diagnosed through surgical intervention due to difficulty in diagnosing the disease before surgery.

Abstract

The primary lymphomas of mucosa associated lymphoid tissue (MALT) of the gallbladder (GB) is an extremely rare of non-Hodgkin lymphoma. Many patients exhibit symptoms like gallstone disease, and in some cases, the lymphoma may be detected through imaging even without apparent symptoms. Only 19 cases of primary MALT lymphoma in the GB have been previously reported. Differential diagnosis from typical GB carcinoma based solely on imaging findings can be challenging, and definitive diagnosis often requires surgical intervention. We present a patient in an 82-year-old man who was initially diagnosed with prostate cancer but incidentally detected GB wall thickening from magnetic resonance imaging conducted for prostatic surgery and subsequent radical cholecystectomy revealed primary MALT lymphoma of the GB. The patient was followed up by a medical oncologist, and after discussion, the decision was made to continue observation with close monitoring without systemic chemotherapy given the asymptomatic presentation. The patient has been free of recurrence for 16 months after the surgery. Although precise diagnosis before the surgery was difficult in this case, preoperative examinations revealed a submucosal tumor-like lesion. MALT lymphoma of GB remains little known in many previous studies. It is really difficult to preoperatively diagnose. The combination of clinical presentation, postoperative histology and immunohistochemistry contribute to diagnosis and carry out appropriate management.

Overview

  • The study reports a rare case of primary mucosa-associated lymphoid tissue (MALT) lymphoma of the gallbladder (GB) in an 82-year-old man.
  • The patient was initially diagnosed with prostate cancer but incidentally detected GB wall thickening from magnetic resonance imaging (MRI) conducted for prostatic surgery.
  • Subsequent radical cholecystectomy revealed primary MALT lymphoma of the GB, which was diagnosed through surgical intervention due to the difficulty in diagnosing the disease before surgery.

Comparative Analysis & Findings

  • The study highlights the importance of combining clinical presentation, postoperative histology, and immunohistochemistry for diagnosing MALT lymphoma of the GB.
  • The patient's asymptomatic presentation and lack of systemic symptoms made it necessary to continue observation with close monitoring without systemic chemotherapy.
  • The study adds to the total of 19 previously reported cases of primary MALT lymphoma in the GB, emphasizing the rarity of this condition.

Implications and Future Directions

  • The study suggests that MALT lymphoma of the GB remains little known and requires further research to understand its diagnosis, treatment, and prognosis.
  • The finding of a submucosal tumor-like lesion on preoperative examinations highlights the importance of careful preoperative examination and evaluation.
  • Future studies should focus on developing diagnostic criteria and treatment strategies for this rare condition, taking into account the patient's asymptomatic presentation and lack of systemic symptoms.