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Spontaneous resolution of transfusion‐associated graft‐versus‐host disease
Author(s) -
Mori S.,
Matsushita H.,
Ozaki K.,
Ishida A.,
Tokuhira M.,
Nakajima H.,
Kizaki M.,
Sugiura H.,
Kikuchi A.,
Handa M.,
Kawai Y.,
Yamamori S.,
Ikeda Y.
Publication year - 1995
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1046/j.1537-2995.1995.35595259155.x
Subject(s) - pancytopenia , medicine , complication , immunology , disease , graft versus host disease , polymerase chain reaction , blood transfusion , leukemia , gastroenterology , bone marrow , biology , gene , biochemistry
BACKGROUND: Transfusion‐associated graft‐versus‐host disease (TA‐GVHD) is a serious complication of blood transfusion that is characterized by high fever, a scaly maculopapular erythematous rash, diarrhea, hepatocellular damage with marked elevation of liver function test values, and pancytopenia. It can occur in immunocompetent as well as immunocompromised recipients. The existence of atypical TA‐GVHD that resolves spontaneously and does not exhibit all of the manifestations has been suggested, but there has been to date no documented diagnosis of GVHD supported by evidence of engraftment. CASE REPORT: A female patient presented and was diagnosed with acute myelogenous leukemia (AML:M4), and, after unsuccessful combination chemotherapy, she received a transfusion and developed manifestation of TA‐GVHD as well as evidence of chimerism. TA‐GVHD was proved by demonstrating Y chromosome‐specific genes in the skin by polymerase chain reaction. The manifestations of clinical GVHD abated within 4 months. CONCLUSION: Polymerase chain reaction analysis of Y chromosomes in specimens from female patients is useful in the diagnosis of suspected cases of spontaneously resolving TA‐GVHD.