Unusual painful pelvic masses: Extramedullary hematopoiesis with extramedullary multiple myeloma
Jennifer Cai, Marian Varda, David Sin, Halline Overby, James J. Yeh

TL;DR
This paper reports a rare case where two blood-related conditions coexist and appear as painful masses in the pelvis, making diagnosis difficult.
Contribution
The paper highlights the rare coexistence of extramedullary hematopoiesis and extramedullary multiple myeloma in a clinical case.
Findings
Extramedullary hematopoiesis and extramedullary multiple myeloma can coexist in the same pelvic mass.
Normal blood cells may outnumber cancerous plasma cells, complicating diagnosis.
CT-guided biopsy and immunohistochemistry are useful for identifying both conditions.
Abstract
The coexistence of extramedullary hematopoiesis and extramedullary multiple myeloma can occur and present as painful pelvic masses. In such a case, normal hematopoietic cells may outnumber clonal plasma cells, posing a diagnostic challenge. Computed tomography‐guided biopsy of the right iliac fossa mass showing extramedullary hematopoiesis with extramedullary multiple myeloma (A, B; yellow arrow: erythroid island; green arrow: myeloid cell; white arrow: megakaryocyte; black arrows: atypical plasma cells with prominent nucleoli; short black arrow: Dutcher body in an atypical plasma cell). CD61 (C) and CD138 (D) immunohistochemistry stains highlight megakaryocytes and plasma cells, respectively.
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsMultiple Myeloma Research and Treatments · Myeloproliferative Neoplasms: Diagnosis and Treatment · Chronic Myeloid Leukemia Treatments
