Journal List > Tuberc Respir Dis > v.67(3) > 1001421

Kim, Kim, Noh, Kang, Chang, Kim, Lee, and Kim: A Case of Extramedullary Hematopoiesis Presenting as a Lung Mass in a Patient with Primary Myelofibrosis

Abstract

Primary myelofibrosis is characterized by replacement of bone marrow with fibrotic tissue and the development of extramedullary hematopoiesis. Extramedullary hematopoiesis primarily involves the spleen and liver, but can also occur in the lungs. We report the case of an 80-year-old male who was admitted for evaluation of a lung mass and persistent thrombocytopenia. A percutaneous needle aspiration from the mass in the right lower lung showed myelopoietic cells with fatty tissue. A bone marrow biopsy revealed a hypercellular marrow with an increased number of atypical megakaryocytes. The final diagnosis was a prefibrotic stage of primary myelofibrosis leading to extramedullary hematopoiesis in the lung.

Figures and Tables

Figure 1
Chest X-ray findings. An airspace opacity was found in the right lower lung.
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Figure 2
Chest CT findings. (A) Ground glass opacities and a 3 cm mass were found in the right lower lung. (B) Mild splenomegaly was noted with multiple low attenuated lesion, which are likely foci of extramedullary hematopoiesis.
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Figure 3
Pathologic findings of percutaneous needle aspiration from the mass in the right lower lung. The myelopoietic cells with fatty tissue were suggestive of extramedullary hematopoiesis (H&E stain, ×400).
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Figure 4
Peripheral blood smear findings. The platelet number was markedly decreased (Wright-Giemsa stain, ×1,000).
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Figure 5
Bone marrow biopsy findings. The marrow revealed hypercellularity (>90%) with an increased number of dysplastic megakaryocytes, including megakaryocytes with hypolobulated nuclei (Wright-Giemsa stain, ×400).
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