Korean J Hematol 1996; 31(1):

Published online March 31, 1996

© The Korean Society of Hematology

파종성 결핵에서 반응성 조직구 식혈증후군을 동반한 범혈구 감소증 1례

박선숙, 강진형, 김치홍, 장은덕

가톨릭대학교 의과대학 성빈센트병원 내과학교실,
가톨릭대학교 의과대학 성빈센트병원 임상병리과학교실

A Case of Pancytopenia Associated with Disseminated Tuberculosis and Reactive Histiocytic Hemophagocytic Syndrome

Sun Sook Park, Jin Hyoung Kang, Chi Hong Kim, Eun Duck Chang

Department of Internal Medicine, Clinical Pathology, St. Vincent Hospital, Catholic University Medical College, Suwon, Korea

Abstract

Miliary tuberculosis is commonly associated with various hematologic changes
including anemia, leukopenia, leukocytosis, monocytosis, leukemoid reaction, basophilia,
disseminated intravascular coagulation, and rarely pancytopenia. Pancytopenia in miliary
tuberculosis has been proven a grave prognostic indicator. The precise mechanism of
pancytopenia in miliary tuberculosis is not known yet and there are still much
controversy. Recently, reactive histiocytic hemophagocytic syndrome was accepted as one
of possible mechanisms of pancytopenia accompanied with miliary tuberculosis
Authors experienced a rare case of pancytopenia and hemophagocytic syndrome
associated with miliary tuberculosis in a 69-year-old female. The bone marrow
examination revealed osseous granulomas with tuberculous bacilli and histiocytic
hemophagocytosis. Despite anti-tuberculosis chemotherapy and active supportive care, the
pancytopenia did not resolved, finally she died of respiratory failure.
Tuberculosis is a common infection in Korea. Therefore, in the presence of
pancytopenia, together with pyrexia and hepatopathy, miliary tuberculosis should always
be considered.

Keywords Miliary tuberculosis, Pancytopenia, Reactive histiocytic hemophagocytic syndrome

Article

Korean J Hematol 1996; 31(1): 167-173

Published online March 31, 1996

Copyright © The Korean Society of Hematology.

파종성 결핵에서 반응성 조직구 식혈증후군을 동반한 범혈구 감소증 1례

박선숙, 강진형, 김치홍, 장은덕

가톨릭대학교 의과대학 성빈센트병원 내과학교실,
가톨릭대학교 의과대학 성빈센트병원 임상병리과학교실

A Case of Pancytopenia Associated with Disseminated Tuberculosis and Reactive Histiocytic Hemophagocytic Syndrome

Sun Sook Park, Jin Hyoung Kang, Chi Hong Kim, Eun Duck Chang

Department of Internal Medicine, Clinical Pathology, St. Vincent Hospital, Catholic University Medical College, Suwon, Korea

Abstract

Miliary tuberculosis is commonly associated with various hematologic changes
including anemia, leukopenia, leukocytosis, monocytosis, leukemoid reaction, basophilia,
disseminated intravascular coagulation, and rarely pancytopenia. Pancytopenia in miliary
tuberculosis has been proven a grave prognostic indicator. The precise mechanism of
pancytopenia in miliary tuberculosis is not known yet and there are still much
controversy. Recently, reactive histiocytic hemophagocytic syndrome was accepted as one
of possible mechanisms of pancytopenia accompanied with miliary tuberculosis
Authors experienced a rare case of pancytopenia and hemophagocytic syndrome
associated with miliary tuberculosis in a 69-year-old female. The bone marrow
examination revealed osseous granulomas with tuberculous bacilli and histiocytic
hemophagocytosis. Despite anti-tuberculosis chemotherapy and active supportive care, the
pancytopenia did not resolved, finally she died of respiratory failure.
Tuberculosis is a common infection in Korea. Therefore, in the presence of
pancytopenia, together with pyrexia and hepatopathy, miliary tuberculosis should always
be considered.

Keywords: Miliary tuberculosis, Pancytopenia, Reactive histiocytic hemophagocytic syndrome

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