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A perplexing primary novel hilar lesion: Remember the pneumonic PPNHL!
Ketaki Utpat1, Unnati D Desai1, Gayathri Amonkar2
1Department of Pulmonary Medicine, TNMC and BYL Nair Hospital, Mumbai, Maharashtra, India.
Indian Journal of Pathology & Microbiology
|March 24, 2018
Summary
Primary pulmonary non-Hodgkin's lymphoma (PPNHL) is a rare cause of hilar masses. This case highlights the diagnostic approach and preferred CHOP chemotherapy regimen for PPNHL.
Area of Science:
- Oncology
- Pulmonology
- Pathology
Background:
- Hilar masses can present with various symptoms including dyspnea, cough, and chest pain.
- Primary pulmonary non-Hodgkin's lymphoma (PPNHL) is an uncommon malignancy affecting the lungs.
- Accurate diagnosis of hilar masses requires a multimodal approach.
Observation:
- A 60-year-old female presented with symptoms suggestive of a left hilar mass.
- Diagnostic workup included clinicoradiological correlation, bronchoscopy, and computed tomography-guided biopsy.
- Histopathology and immunohistochemistry confirmed the diagnosis of PPNHL.
Findings:
- The case identified primary pulmonary non-Hodgkin's lymphoma (PPNHL) as the cause of the left hilar mass.
- Mucosa-associated lymphoid tissue (MALT) lymphoma is the most common subtype of PPNHL.
- The study emphasizes the importance of integrating clinical, radiological, and pathological findings.
Implications:
- This case underscores the diagnostic challenges and considerations for evaluating hilar masses.
- Early and accurate diagnosis of PPNHL is crucial for effective treatment.
- The cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) chemotherapy regimen is a preferred treatment option for PPNHL.
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