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Primary pulmonary lymphoma in Peru

OBJECTIVE: To describe the clinical features, imaging, pathology and management of patients with primary pulmonary lymphoma (PPL). METHODOLOGY: This is a case series study involving a retrospective analysis of 24 patients diagnosed with PPL between the years 2000–2019 at Instituto Nacional de Enferm...

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Detalles Bibliográficos
Autores principales: Requena, Elily Dianet Apumayta, Ocrospoma, Danery Valdez, Ruiz, Jhonatanael Salvador, De la Guerra Pancorvo, Alberto, Kajatt, Edgar Amorin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310327/
https://www.ncbi.nlm.nih.gov/pubmed/37396099
http://dx.doi.org/10.3332/ecancer.2023.1559
Descripción
Sumario:OBJECTIVE: To describe the clinical features, imaging, pathology and management of patients with primary pulmonary lymphoma (PPL). METHODOLOGY: This is a case series study involving a retrospective analysis of 24 patients diagnosed with PPL between the years 2000–2019 at Instituto Nacional de Enfermedades Neoplásicas in Lima, Perú. RESULTS: 73.9% of patients were male. Cough (78.3%) and weight loss (56.5%) were the most frequent clinical features. Dyspnoea and elevated values of DHL and B2 microglobulin were frequently altered in advanced stages. Diffuse large B cell lymphoma (DLBCL) represented 47.8% of the cases and the most common radiologic alterations were a mass (60%) and consolidation with air bronchogram (60%). The most utilised treatment was chemotherapy alone (60%). Three patients received only surgery. Median survival was 30 months. Five overall survival was 45%, and up to 60% in the case of mucosa-associated lymphoid tissue lymphoma. CONCLUSION: PPL is infrequent. Clinical features are unspecific and the principal finding is a mass, nodule or consolidation with air bronchogram. Definitive diagnosis needs biopsy and immunohistochemistry. There is no standard treatment, it depends on histology type and stage.