Literature DB >> 22959233

Histopathology and correlates of systemic disease in adult Henoch-Schönlein purpura: a retrospective study of microscopic and clinical findings in 68 patients at Mayo Clinic.

Timothy J Poterucha1, David A Wetter, Lawrence E Gibson, Michael J Camilleri, Christine M Lohse.   

Abstract

BACKGROUND: The histopathology of Henoch-Schönlein purpura (HSP) is well defined, but specific markers have not been correlated with systemic involvement.
OBJECTIVE: We sought to evaluate whether histopathologic markers were associated with renal or other systemic involvement in adult HSP.
METHODS: We retrospectively reviewed clinical information and pathology slides of 68 adult patients with HSP seen at Mayo Clinic between 1992 and 2011.
RESULTS: Of the 68 patients, mean age was 45.8 years and 41 (60%) of the patients were male. Renal involvement was observed in 30 patients (44%), gastrointestinal tract in 27 (40%), joint in 32 (47%), and any systemic signs in 52 (76%). Patients who were older than 40 years and had leukocytoclastic vasculitis with an absence of eosinophils on skin biopsy specimen had higher rates of renal involvement than those who did not have both of these features (75% vs 27%; P < .001). Patients with skin biopsy specimens showing leukocytoclastic vasculitis and an absence of histiocytes had higher rates of gastrointestinal tract involvement (P = .03). Age of 40 years or younger was associated with increased risk for gastrointestinal tract involvement and a nonsignificant trend for joint involvement (P = .004 and P = .06, respectively). LIMITATIONS: This study is retrospective, and the causative factors of HSP were unable to be determined in many patients.
CONCLUSION: Patients older than 40 years with HSP who had an absence of eosinophils on skin biopsy specimen had a nearly 3-times increased risk of renal involvement compared with patients who did not have both features.
Copyright © 2012 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22959233     DOI: 10.1016/j.jaad.2012.08.011

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  8 in total

1.  Real-time vascular and IgA dynamics during Henoch-Schönlein purpura by in vivo fluorescent microscopy.

Authors:  Yujie Zhu; Shaoyang Wang; Hui Xu; Hao He; Meng Pan
Journal:  Biomed Opt Express       Date:  2021-11-29       Impact factor: 3.732

Review 2.  Cutaneous vasculitis: a rheumatologist perspective.

Authors:  Trinitario Pina; Ricardo Blanco; Miguel A González-Gay
Journal:  Curr Allergy Asthma Rep       Date:  2013-10       Impact factor: 4.919

3.  Bullous skin lesions in an adult male: a diagnostic dilemma.

Authors:  Gaurav Gulati; Jenny Siv; Avis E Ware
Journal:  Am J Case Rep       Date:  2015-04-10

4.  Histologic characterization of cellular infiltration in autoimmune subepidermal bullous diseases in a tertiary hospital in Saudi Arabia.

Authors:  Hessah F BinJadeed; Alanoud M Alyousef; Fahad M Alsaif; Ahmed A Alhumidi; Homaid O Alotaibi
Journal:  Clin Cosmet Investig Dermatol       Date:  2018-04-24

5.  Gastrointestinal Biopsy in Henoch-Schönlein Purpura: A Great Diagnostic Contribution.

Authors:  Imen Akkari; Soumaya Mrabet; Elhem Ben Jazia
Journal:  Eur J Case Rep Intern Med       Date:  2017-09-27

6.  Indian scenario of IgA nephropathy: a systematic review and meta-analysis.

Authors:  Anju Khairwa
Journal:  Afr Health Sci       Date:  2021-03       Impact factor: 0.927

7.  Anaphylactoid Purpura Associated with Streptococcal Cellulitis: A Case Report and Literature Review.

Authors:  Yuko Saito; Susumu Ookawara; Hisataka Uchima; Takeshi Ishida; Masafumi Kakei; Hitoshi Sugawara
Journal:  Case Rep Med       Date:  2017-08-16

8.  Blistering eruptions with tissue eosinophilia in a child with IgA vasculitis.

Authors:  Toru Watanabe; Shinya Tsukano
Journal:  Clin Case Rep       Date:  2018-06-04
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.