Systemic mastocytosis: a case report. Cytological, cytochemical and ultrastructural considerations.

Abstract:

:A case of systemic mastocytosis with unusual clinical manifestations, appearing as an isolated splenohepatomegaly, is described. The proliferative character is evident from the cytological characteristics of immaturity and the presence of a moderate percentage of mast cells in the peripheral blood. These cells make up 40% of the total cells in the bone marrow. Special attention is given to the optical, morphological, cytochemical, and ultrastructural studies of the disease. Some anomalies were found at the subcellular level which apparetnly have not been recorded until present. Various dyshematopoietic features of this case are reported, which may be considered as manifestations of a paraneoplastic syndrome.

journal_name

Acta Haematol

journal_title

Acta haematologica

authors

Woessner S,Lafuente R,Pardo P,Rosell R,Rozman C,Sans-Sabrafen J

doi

10.1159/000207846

subject

Has Abstract

pub_date

1977-01-01 00:00:00

pages

321-31

issue

6

eissn

0001-5792

issn

1421-9662

journal_volume

58

pub_type

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