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Case Report

Generalized Lymphadenopathy Secondary to Isolated Extramedullary Hematopoiesis as an Initial Manifestation of Primary Myelofibrosis

by
Mansour S. Aljabry
1,*,
Shuaa Asiri
2,
Tayseer Elsafi
3 and
Ghaleb Elyamany
2
1
Pathology Department, King Khalid University Hospital, King Saud University, P.O. Box 2925, Riyadh 11461, Saudi Arabia
2
Department of Central Military Laboratory and Blood Bank, Prince Sultan Military Medical City, P.O. Box 2925, Riyadh 11461, Saudi Arabia
3
Department of General Medicine, Prince Sultan Military Medical City, P.O. Box 2925, Riyadh 11461, Saudi Arabia
*
Author to whom correspondence should be addressed.
Hematol. Rep. 2018, 10(2), 7588; https://doi.org/10.4081/hr.2018.7588
Submission received: 24 January 2018 / Revised: 3 May 2018 / Accepted: 7 May 2018 / Published: 15 May 2018

Abstract

Extramedullary hematopoiesis (EMH) is a presence of hematopoietic activity in the extramedullary sites. EMH can occur in both benign and malignant hematologic diseases. The liver and spleen are the most common sites, but may also occur infrequently at other sites. EMH often occurs in more than one site and quite rare in an isolated organ. In this study we describe an unusual case of generalized lymphadenopathy secondary to isolated extramedullary hematopoiesis as an initial manifestation of primary myelofibrosis. Computed tomography revealed generalized lymphadenopathy including mediastinal, abdominal and pelvic lymph nodes with extensive illdefined sclerotic lesions throughout the skeletal system suggestive of lymphoma/leukemia. Lymph node biopsy showed no evidence of malignancy or granuloma, however, large abnormal cells with multilobated nuclei were seen scattered in the lymph nodes. These abnormal cells were proved to be megakaryocytes. Granulocytic precursors were less obvious on the H&E section. The diagnosis was determined as EMH in the lymph node. Bone marrow (BM) examination showed hypercellular marrow for patient’s age with granulocytic and megakaryocytic proliferation with increase in BM fibrosis and reported as a myeloproliferative neoplasm, consistent with primary myelofibrosis. In summary, although EMH is not always a malignant process; it is important to stress that the patient should be investigated for underlying hematological disorders, when it is noted elsewhere.
Keywords: lymph node; extramedullary hematopoiesis; myelofibrosis lymph node; extramedullary hematopoiesis; myelofibrosis

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MDPI and ACS Style

Aljabry, M.S.; Asiri, S.; Elsafi, T.; Elyamany, G. Generalized Lymphadenopathy Secondary to Isolated Extramedullary Hematopoiesis as an Initial Manifestation of Primary Myelofibrosis. Hematol. Rep. 2018, 10, 7588. https://doi.org/10.4081/hr.2018.7588

AMA Style

Aljabry MS, Asiri S, Elsafi T, Elyamany G. Generalized Lymphadenopathy Secondary to Isolated Extramedullary Hematopoiesis as an Initial Manifestation of Primary Myelofibrosis. Hematology Reports. 2018; 10(2):7588. https://doi.org/10.4081/hr.2018.7588

Chicago/Turabian Style

Aljabry, Mansour S., Shuaa Asiri, Tayseer Elsafi, and Ghaleb Elyamany. 2018. "Generalized Lymphadenopathy Secondary to Isolated Extramedullary Hematopoiesis as an Initial Manifestation of Primary Myelofibrosis" Hematology Reports 10, no. 2: 7588. https://doi.org/10.4081/hr.2018.7588

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