Thrombocytopenia in hepatitis A - An atypical presentation

Rathika D. Shenoy; Sajitha Nair; Nutan Kamath

doi:10.1093/tropej/50.4.241

Thrombocytopenia in hepatitis A - An atypical presentation

Rathika D. Shenoy^*
, Sajitha Nair
, Nutan Kamath

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

27 Citations (Scopus)

Abstract

Acute hepatitis due to hepatitis A virus (HAV) is usually a benign self-limiting disease during childhood. Autoimmune manifestations are rare with acute HAV, especially in children. We report an 8-year-old boy with severe thrombocytopenia as an initial manifestation of acute HAV infection. Bone marrow examination suggested peripheral destruction of platelets. His clinical course was complicated by persistent severe thrombocytopenia and progressive cholestasis requiring prednisolone therapy.

Original language	English
Pages (from-to)	241-242
Number of pages	2
Journal	Journal of Tropical Pediatrics
Volume	50
Issue number	4
DOIs	https://doi.org/10.1093/tropej/50.4.241
Publication status	Published - 01-08-2004

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health
Infectious Diseases

Access to Document

10.1093/tropej/50.4.241

Cite this

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title = "Thrombocytopenia in hepatitis A - An atypical presentation",

abstract = "Acute hepatitis due to hepatitis A virus (HAV) is usually a benign self-limiting disease during childhood. Autoimmune manifestations are rare with acute HAV, especially in children. We report an 8-year-old boy with severe thrombocytopenia as an initial manifestation of acute HAV infection. Bone marrow examination suggested peripheral destruction of platelets. His clinical course was complicated by persistent severe thrombocytopenia and progressive cholestasis requiring prednisolone therapy.",

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AU - Kamath, Nutan

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N2 - Acute hepatitis due to hepatitis A virus (HAV) is usually a benign self-limiting disease during childhood. Autoimmune manifestations are rare with acute HAV, especially in children. We report an 8-year-old boy with severe thrombocytopenia as an initial manifestation of acute HAV infection. Bone marrow examination suggested peripheral destruction of platelets. His clinical course was complicated by persistent severe thrombocytopenia and progressive cholestasis requiring prednisolone therapy.

AB - Acute hepatitis due to hepatitis A virus (HAV) is usually a benign self-limiting disease during childhood. Autoimmune manifestations are rare with acute HAV, especially in children. We report an 8-year-old boy with severe thrombocytopenia as an initial manifestation of acute HAV infection. Bone marrow examination suggested peripheral destruction of platelets. His clinical course was complicated by persistent severe thrombocytopenia and progressive cholestasis requiring prednisolone therapy.

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AN - SCOPUS:4344588861

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JO - Journal of Tropical Pediatrics

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ER -

Thrombocytopenia in hepatitis A - An atypical presentation

Abstract

UN SDGs

All Science Journal Classification (ASJC) codes

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