Clinical and histopathologic features of 8 patients with microscopic polyangiitis including two with a slowly progressive clinical course - 19/08/11
, Takeshi Kawanabe, MD, PhD a, Chihiro Saito, MD a, Maya Kannari, MD a, Masako Mizoguchi, MD, PhD a, Hiroko Nagafuchi, MD, PhD b, Takahiro Okazaki, MD, PhD b, Shoichi Ozaki, MD, PhD b, Kenjiro Kimura, MD, PhD c, Yoshinao Soma, MD, PhD a
Reprint requests: Tamihiro Kawakami, MD, PhD, Department of Dermatology, St Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, Kanagawa 216-8511, Japan.Abstract |
Background |
Microscopic polyangiitis (MPA) is a systemic antineutrophil cytoplasmic autoantibody–associated vasculitis associated with necrotizing and crescentic glomerulonephritis and pulmonary capillaritis. MPA generally has a rapidly progressive clinical course, but there have been recent reports of slowly progressive cases.
Objective |
To evaluate the typical cutaneous findings of MPA, we recorded the clinical and histopathologic features of the cutaneous manifestations.
Methods |
Eight patients with MPA, who had presented with cutaneous manifestations between 2001 and 2005 in our department, were retrospectively reviewed. They had necrotizing vasculitis in their cutaneous lesions as confirmed by skin biopsy specimens. Patients with other known connective tissue diseases were not included in the study.
Results |
All 8 patients with MPA presented cutaneously with erythematous macules on their extremities. Livedo reticularis (5/8, 68%) was also observed. Six of the 8 patients with MPA were given the diagnosis within 3 months of their initial manifestation. In skin biopsy specimens, necrotizing vasculitis was noted in the reticular dermis to the subcutaneous fat. In contrast, the other two patients with MPA were given the diagnosis about 10 years after their initial manifestation. Histopathologic findings demonstrated necrotizing vasculitis with moderate neutrophilic infiltrations in the papillary to middle dermis in the latter two patients. Serum myeloperoxidase-antineutrophil cytoplasmic autoantibody levels were only moderlately elevated in the latter two patients and they were given the diagnosis of slowly progressive MPA. Histopathologically, palisading granulomas were present on the elbow of one of them.
Limitations |
The study was based on histopathological analysis in a limited number of patients due to the rareness of the investigated disease.
Conclusions |
There appears to be a correlation between a slowly progressive clinical course of MPA and the depth of dermal involvement and the severity of neutrophilic infiltration in biopsy specimens. Based on these results, we believe that these characteristic patterns may help clinicians establish an earlier diagnosis of possible MPA with positive antineutrophil cytoplasmic autoantibody titers.
Le texte complet de cet article est disponible en PDF.Abbreviations used : ANCA, CHCC, CRP, CSS, CT, ESR, MPA, MPO, NV, PR3-ANCA
Plan
| Supported by grants from the Scientific Research Fund of the Ministry of Education, Science, Sports, and Culture, Japan (Grants-in-Aid for Scientific Research No. 14570828, 16591121, and 18591261). |
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| Conflicts of interest: None declared. |
Vol 57 - N° 5
P. 840-848 - novembre 2007 Retour au numéro
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