Cytomegalovirus-associated pulmonary septal capillary injury sine inclusion body change: a distinctive cause of occult or macroscopic pulmonary hemorrhage in the immunocompetent host.

TitleCytomegalovirus-associated pulmonary septal capillary injury sine inclusion body change: a distinctive cause of occult or macroscopic pulmonary hemorrhage in the immunocompetent host.
Publication TypeJournal Article
Year of Publication2005
AuthorsMagro C, Ali N, Williams JAD, Allen JN, Ross P
JournalAppl Immunohistochem Mol Morphol
Volume13
Issue3
Pagination268-72
Date Published2005 Sep
ISSN1541-2016
KeywordsCapillaries, Cytomegalovirus, Cytomegalovirus Infections, Female, Ganciclovir, Glomerulonephritis, Hemorrhage, Humans, Immediate-Early Proteins, Immunocompromised Host, Inclusion Bodies, Viral, Lung, Lung Diseases, Male, Middle Aged, RNA, Viral, Steroids, Thrombocytopenia, Viral Proteins
Abstract

The authors describe four patients with symptomatic lung disease morphologically representing a septal capillary injury syndrome temporally associated with serologic and culture evidence of active cytomegalovirus (CMV) infection but without classic cytopathic changes. The authors conducted a thorough review of clinical data, microscopic examination, and in situ hybridization to detect CMV mRNA encoding immediate early protein. The assay detects transcripts that encode early and immediate early proteins. In two cases additional tissue was available for direct immunofluorescent studies. The disease process in each of the patients was morphologically indistinguishable from the pattern of organ injury associated with autoimmune diseases including a small vessel microvascular injury syndrome involving skin and lung and immune complex- mediated glomerulonephritis. Cytopenias were seen in all cases, most commonly thrombocytopenia. All treated patients demonstrated improvement on combined ganciclovir and low-dose steroid therapy. CMV infection may be of pathogenetic importance in some cases of alveolar hemorrhage, especially when accompanied by peripheral blood cytopenia in otherwise healthy patients and if clinical worsening occurs in the setting of a traditional immunosuppressive regimen typically used to treat vasculitis.

DOI10.1097/01.pai.0000137911.39736.95
Alternate JournalAppl Immunohistochem Mol Morphol
PubMed ID16082254
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