Abstract

BackgroundExtramedullary plasmacytoma is a rare monoclonal plasma cell neoplasm that originates from tissues other than the bone marrow and constitutes only 3%–5% of all plasma cell neoplasms. Most cases involve the upper respiratory tract. Extramedullary plasmacytoma involving the lung is extremely rare. Primary pulmonary plasmacytoma is a rare type of extramedullary plasmacytoma, usually presenting with a nodule or mass in hilar region. Literature search has shown very few cases of immunohistochemically confirmed cases of pulmonary plasmacytoma. Diffuse pulmonary infiltration is an unusual presentation.Case presentationWe report the case of a 56 year old lady with history of cough and breathlessness since one month. Computed Tomography revealed diffusely scattered multiple cavitating nodules and consolidation in both lungs. Computed Tomography guided biopsy of one of the lung nodules was done. Histopathologic examination and immunohistochemistry showed features of pulmonary plasmacytoma .This is an unique case of primary pulmonary plasmacytoma with the rare presentation as diffusely scattered multiple cavitating nodules and consolidation. According to our literature search, primary pulmonary plasmacytoma manifesting as cavitating nodules is being reported for the first time.ConclusionsPrimary pulmonary plasmacytoma should be also be considered in the differential diagnosis of multiple diffusely scattered cavitating lung nodules.

Highlights

  • Extramedullary plasmacytoma is a rare monoclonal plasma cell neoplasm that originates from tissues other than the bone marrow and constitutes only 3%–5% of all plasma cell neoplasms

  • Primary pulmonary plasmacytoma should be be considered in the differential diagnosis of multiple diffusely scattered cavitating lung nodules

  • Extramedullary plasmacytoma (EMP) is a monoclonal plasma cell tumour that originates from tissues other than the bone marrow [1]

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Summary

Background

Extramedullary plasmacytoma (EMP) is a monoclonal plasma cell tumour that originates from tissues other than the bone marrow [1]. We report a case of PPP presenting as diffusely distributed. The chest radiograph showed multifocal diffuse confluent nodular opacities in both lungs and consolidation in bilateral lower zones. High resolution computed tomography scan (HRCT) revealed multiple discrete and confluent solid as well as ground glass nodules diffusely scattered in both lungs, predominantly in lower lobes .Most of the nodules showed central cavitation. No lytic lesions were seen in spine and bony thoracic cage. Microscopy on histopathology (Fig 3a) showed features suggestive of small round cell tumor with differential diagnosis as plasmacytoma and neuroendocrine tumor. Immunohistochemistry (Fig 3b) revealed neoplastic plasma cells showing strong diffuse expression of CD138, CD45, vimentin and kappa, focally positive

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