Splenic Mastocytosis

Author:

ENDE NORMAN1,CHERNISS EDWARD I.1

Affiliation:

1. Laboratory Service, Medical Service and Research Laboratory, V.A. Hospital, Fresno, California.

Abstract

Abstract 1. A patient with splenic mastocytosis who had hypersplenism, periodic flushing and clotting defects is presented. 2. A correlation is shown between mastocytosis and elevated histamine and heparin levels in the spleen. 3. The patient is well nine months after splenectomy. 4. Wright’s stain or polychrome methylene blue stain of splenic tissue imprints is recommended as a method of demonstrating mast cells in the spleen. 5. Mast cell counts of normal spleen showed 0 to 0.25% of nucleated cells on imprint. 6. Splenic aspiration stained with Wright’s stain is satisfactory for demonstrating mastocytosis, though not dependable for true mast cell counts. 7. Cases of primary hypersplenism should routinely be reviewed for splenic mastocytosis. 8. Splenic mastocytosis is a variant of systemic mast cell disease in which involvement is predominately confined to the spleen.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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1. Beyond the Usual Suspects: Unraveling Spleen Mastocytosis in Hypersplenism Differential Diagnosis;Cureus;2024-08-18

2. Systemic Mastocytosis and Mast Cell Tumors;Tumors and Tumor-Like Lesions of the Hepatobiliary Tract;2016-10-20

3. Systemic Mastocytosis and Mast Cell Tumors;Tumors and Tumor-Like Lesions of the Hepatobiliary Tract;2016

4. Malignant Systemic Mast Cell Disease (Mastocytoma) in Man;Acta Medica Scandinavica;2009-04-24

5. SYSTEMIC MASTOCYTOSIS WITHOUT CUTANEOUS INVOLVEMENT;Pathology International;2008-12-12

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