Pulmonary extra‐nodal mucosa‐associated lymphoid tissue (MALT) lymphoma: A rare cause of persistent lung consolidation

Author:

Kou Lily1,Huan Nai‐Chien2ORCID,Nyanti Larry Ellee3ORCID,Chin Jiunn Sheng1,Mohamad Nor Bahiyyah4,Ramarmuty Hema Yamini2

Affiliation:

1. Department of Medicine Keningau Hospital Keningau Malaysia

2. Department of Respiratory Medicine Queen Elizabeth Hospital Kota Kinabalu Malaysia

3. Medical Department, Faculty of Medicine and Health Sciences Universiti Malaysia Sabah Kota Kinabalu Malaysia

4. Department of Pathology Queen Elizabeth Hospital Kota Kinabalu Malaysia

Abstract

AbstractPulmonary extra‐nodal marginal zone B‐cell lymphoma, also known as extra‐nodal mucosa‐associated lymphoid tissue (MALT) lymphoma, is rare among all non‐Hodgkin lymphomas and generally among all pulmonary malignancies. We present a 46‐year‐old lady with persistent right lower lung consolidation despite earlier treatment efforts with intravenous antibiotics for community acquired pneumonia. Apart from initial presentation with a short 3‐day history of fever, cough and shortness of breath, she had remained largely asymptomatic throughout the follow‐up period. Flexible bronchoscopy done ruled out infectious aetiologies but transbronchial lung biopsies showed atypical lymphocytes. A computed tomography guided core biopsy of her right lung consolidation was subsequently performed, confirming a diagnosis of pulmonary MALT lymphoma. She was promptly referred to the haematology team for further management and commencement of chemotherapy. Pulmonary MALT lymphoma, albeit uncommon and often follows a relatively indolent cause, should be considered as a differential diagnosis among patients with persistent lung consolidation.

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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