Chronic Mastitis in Egypt and Morocco

Differentiating between Idiopathic Granulomatous Mastitis and IgG4-Related Disease

Steven G. Allen, Amr S. Soliman, Kathleen Toy, Omar S. Omar, Tamer Youssef, Mehdi Karkouri, Essam Ayad, Azza Abdel-Aziz, Ahmed Hablas, Ali Tahri, Hanna N. Oltean, Celina G. Kleer, Sofia D. Merajver

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Idiopathic granulomatous mastitis (IGM) is a benign, frequently severe chronic inflammatory lesion of the breast. Its etiology remains unknown and reported cases vary in their presentation and histologic findings with an optimal treatment algorithm yet to be described owing mainly to the disease's heterogeneity. IgG4-related disease (IgG4-RD) is a newly recognized systemic fibroinflammatory condition characterized by a dense lymphoplasmacytic infiltrate with many IgG4-positive plasma cells, storiform fibrosis, and obliterative phlebitis. Immunosuppressive therapy is considered to be an effective first-line therapy for IgG4-RD. We sought to clarify and classify chronic mastitis according to the histologic findings of IgG4-RD mastitis with respect to IGM and to develop a robust diagnostic framework to help select patients for optimal treatment strategies. Using the largest collection to date (43 cases from Egypt and Morocco), we show that despite sharing many features, IGM and IgG4-RD mastitis are separate diseases. To diagnostically separate the diseases, we created a classification schema—termed the Michigan Classification—based upon our large series of cases, the consensus statement on IgG4-RD, and the histologic description of IGM in the literature. Using our classification, we discerned 17 cases of IgG4-RD and 8 cases of IGM among the 43 chronic mastitis cases, with 18 indeterminate cases. Thus, our Michigan Classification can form the basis of rational stratification of chronic mastitis patients between these two clinically and histopathologically heterogeneous diseases.

Original languageEnglish (US)
Pages (from-to)501-509
Number of pages9
JournalBreast Journal
Volume22
Issue number5
DOIs
StatePublished - Sep 1 2016

Fingerprint

Granulomatous Mastitis
Morocco
Mastitis
Egypt
Immunoglobulin G
Phlebitis
Therapeutics
Immunosuppressive Agents
Plasma Cells

Keywords

  • Idiopathic granulomatous mastitis
  • IgG4-related disease
  • mastitis

ASJC Scopus subject areas

  • Internal Medicine
  • Surgery
  • Oncology

Cite this

Allen, S. G., Soliman, A. S., Toy, K., Omar, O. S., Youssef, T., Karkouri, M., ... Merajver, S. D. (2016). Chronic Mastitis in Egypt and Morocco: Differentiating between Idiopathic Granulomatous Mastitis and IgG4-Related Disease. Breast Journal, 22(5), 501-509. https://doi.org/10.1111/tbj.12628

Chronic Mastitis in Egypt and Morocco : Differentiating between Idiopathic Granulomatous Mastitis and IgG4-Related Disease. / Allen, Steven G.; Soliman, Amr S.; Toy, Kathleen; Omar, Omar S.; Youssef, Tamer; Karkouri, Mehdi; Ayad, Essam; Abdel-Aziz, Azza; Hablas, Ahmed; Tahri, Ali; Oltean, Hanna N.; Kleer, Celina G.; Merajver, Sofia D.

In: Breast Journal, Vol. 22, No. 5, 01.09.2016, p. 501-509.

Research output: Contribution to journalArticle

Allen, SG, Soliman, AS, Toy, K, Omar, OS, Youssef, T, Karkouri, M, Ayad, E, Abdel-Aziz, A, Hablas, A, Tahri, A, Oltean, HN, Kleer, CG & Merajver, SD 2016, 'Chronic Mastitis in Egypt and Morocco: Differentiating between Idiopathic Granulomatous Mastitis and IgG4-Related Disease', Breast Journal, vol. 22, no. 5, pp. 501-509. https://doi.org/10.1111/tbj.12628
Allen, Steven G. ; Soliman, Amr S. ; Toy, Kathleen ; Omar, Omar S. ; Youssef, Tamer ; Karkouri, Mehdi ; Ayad, Essam ; Abdel-Aziz, Azza ; Hablas, Ahmed ; Tahri, Ali ; Oltean, Hanna N. ; Kleer, Celina G. ; Merajver, Sofia D. / Chronic Mastitis in Egypt and Morocco : Differentiating between Idiopathic Granulomatous Mastitis and IgG4-Related Disease. In: Breast Journal. 2016 ; Vol. 22, No. 5. pp. 501-509.
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