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Clinical Rheumatology

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13.04.2019 | Case Based Review

Exceptional association of hypocomplementemic urticarial vasculitis syndrome (HUVS) and symptomatic pulmonary histoplasmosis: a case-based literature review

verfasst von: Mohammad Alomari, Laith Al Momani, Shrouq Khazaaleh, Shaden Almomani, Kinanah Yaseen, Bassam Alhaddad

Erschienen in: Clinical Rheumatology | Ausgabe 6/2019

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Abstract

Hypocomplementemic urticarial vasculitis syndrome (HUVS) is a rare type III hypersensitivity disorder characterized by urticarial vasculitis and prolonged hypocomplementemia. Individuals with HUVS may also have joint involvement, pulmonary manifestations, ocular disease, kidney inflammation, or any other form of organ involvement. Hypocomplementemia, the presence of C1q antibody in the serum, and urticarial vasculitis are the keys to the diagnosis of HUVS. It has been reported to accompany certain infections such as hepatitis B, hepatitis C, infectious mononucleosis, and coxsackie group A. However, it has never been reported to be linked to histoplasmosis in the literature. To the best of our knowledge, we report the first case of HUVS presenting concurrently with pulmonary histoplasmosis.

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Titel: Exceptional association of hypocomplementemic urticarial vasculitis syndrome (HUVS) and symptomatic pulmonary histoplasmosis: a case-based literature review
verfasst von: Mohammad Alomari
Laith Al Momani
Shrouq Khazaaleh
Shaden Almomani
Kinanah Yaseen
Bassam Alhaddad
Publikationsdatum: 13.04.2019
Verlag: Springer London
Erschienen in: Clinical Rheumatology / Ausgabe 6/2019
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI: https://doi.org/10.1007/s10067-019-04548-8

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Exceptional association of hypocomplementemic urticarial vasculitis syndrome (HUVS) and symptomatic pulmonary histoplasmosis: a case-based literature review

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