Pulmonary MALT Cell Lymphoma Mimicking as ILD

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dc.contributor.authorGupta, Rishabhen_US
dc.contributor.authorPrajapat, Deepaken_US
dc.contributor.authorSingh, Kanishka Ken_US
dc.contributor.authorPrakash, Anupamen_US
dc.contributor.authorTalwar, Deepaken_US
dc.date.accessioned2024-12-07T11:59:02Z
dc.date.available2024-12-07T11:59:02Z
dc.date.issued2024-09
dc.description.abstractAim and background: The aim is to illustrate the diagnostic challenge posed by pulmonary mucosa-associated lymphoid tissue (MALT) cell lymphoma, which can mimic interstitial lung disease (ILD). Representing 0.5–1% of lung neoplasia cases, primary pulmonary lymphomas, particularly MALT lymphomas, present diagnostic challenges due to varied imaging features and lack of specific biological markers. This case report highlights the diagnostic complexities when pulmonary MALT cell lymphoma mimics ILD, emphasizing the need for accurate histopathological confirmation. Case description: A 50-year-old female initially diagnosed and treated for ILD based on radiological findings, presented with worsening breathlessness and a dry cough. Examination revealed fine crackles in both lung fields, and imaging indicated reticular opacities suggesting ILD. Laboratory tests showed elevated serum lactate dehydrogenase and a positive ANA in autoimmune profiling. Despite treatment, symptoms worsened. Subsequent transbronchial biopsy confirmed pulmonary MALT cell lymphoma, prompting Rituximab therapy after multidisciplinary consultation. Conclusion: This case underscores the challenge of distinguishing between pulmonary MALT cell lymphoma and ILD solely based on radiological similarities. Accurate histopathological diagnosis through biopsies is pivotal in managing such cases effectively. Multidisciplinary collaboration facilitated a precise diagnosis and appropriate therapy, emphasizing its crucial role in managing complex conditions. Clinical significance: The case demonstrates the diagnostic complexity of differentiating pulmonary MALT cell lymphoma from ILD, stressing the necessity of histopathological confirmation. An accurate diagnosis significantly influences therapy prognosis and highlights the indispensable role of multidisciplinary collaboration in managing such rare cases.en_US
dc.identifier.affiliationsDepartment of Pulmonary, Sleep & Critical Care Medicine, Metro Group of Hospitals, Noida, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Pulmonary, Sleep & Critical Care Medicine, Metro Group of Hospitals, Noida, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Pulmonary, Sleep & Critical Care Medicine, Metro Group of Hospitals, Noida, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Pulmonary, Sleep & Critical Care Medicine, Metro Group of Hospitals, Noida, Uttar Pradesh, Indiaen_US
dc.identifier.affiliationsDepartment of Pulmonary, Sleep & Critical Care Medicine, Metro Group of Hospitals, Noida, Uttar Pradesh, Indiaen_US
dc.identifier.citationGupta Rishabh, Prajapat Deepak, Singh Kanishka K, Prakash Anupam, Talwar Deepak . Pulmonary MALT Cell Lymphoma Mimicking as ILD . The Indian Journal of Chest Diseases and Allied Sciences. 2024 Sep; 66(3): 97-101en_US
dc.identifier.issn0377-9343
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/242306
dc.languageenen_US
dc.publisherJaypee Brothers Medical Publishers Pvt. Ltd.en_US
dc.relation.issuenumber3en_US
dc.relation.volume66en_US
dc.source.urihttps://doi.org/10.5005/jp-journals-11007-0127en_US
dc.subjectCase reporten_US
dc.subjectInterstitial lung diseaseen_US
dc.subjectMisdiagnosisen_US
dc.subjectPulmonary malt cell lymphomaen_US
dc.titlePulmonary MALT Cell Lymphoma Mimicking as ILDen_US
dc.typeJournal Articleen_US
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