Results 81 to 90 of about 207 (118)
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Clinicopathologic and immunophenotypic features of eosinophilic fasciitis and morphea profunda: A comparative study of 27 cases

Journal of the American Academy of Dermatology, 2018
Eosinophilic fasciitis (EF) and morphea profunda (MP) are inflammatory and sclerosing disorders of the subcutis that can exhibit clinical and pathologic presentations that overlap.To identify clinicopathologic features that can be used to distinguish EF from MP.We performed a retrospective review of 16 patients with EF and 11 patients with MP ...
Oluwakemi, Onajin   +4 more
openaire   +2 more sources

Solitary Morphea Profunda in a 5‐Year‐Old Girl: Case Report and Review of the Literature

Pediatric Dermatology, 1991
Abstract: A 5‐year‐old girl had a solitary sclerotic plaque on the back of recent onset. The histopathologic features were consistent with morphea profunda. Thickening and homogenization of collagen bundles were demonstrated in the dermis and subcutaneous tissues, admixed with a prominent lymphocytic and plasma cell inflammatory infiltrate.
K A, Kobayashi, H, Lui, J S, Prendiville
openaire   +2 more sources

Pediatric‐onset solitary morphea profunda

International Journal of Dermatology, 2020
Takashi Ito   +3 more
openaire   +2 more sources

[Plasma cell panniculitis: a histopathological variant of morphea profunda].

Annales de dermatologie et de venereologie, 2009
Plasma cell panniculitis is a rare histopathological variant of morphea profunda. Its occurrence in two siblings has been reported once. We report a new case in which a brother and a sister with a family history of consanguinity presented plasma cell panniculitis of long duration.A man and his sister, 38 and 28 years old respectively, presented thick ...
R, Tomb, B, Soutou, S, Chehadi
openaire   +1 more source

Hydroxychloroquine combined with superficial X‐ray—A new therapeutic method in the treatment of morphea profunda

Dermatologic Therapy, 2019
Morphea profunda (MP) is a variant of morphea that presents clinically as localized fibrotic plaques. Based on previous reports, there was no unified standard treatment for MP. Here we report a rare case of MP, which is the first report about treatment by hydroxychloroquine in combination with superficial X-ray.
Chao Li   +3 more
openaire   +2 more sources

Nodular morphea (NM): report of a case of concurrent NM and morphea profunda associated with limited type systemic sclerosis, and overview and definition for NM

European Journal of Dermatology, 2013
Morphea consists of various variants, including nodular morphea (NM), keloidal morphea (KM) and morphea profunda (MP). NM and KM are used synonymously. We present a 67-year-old Japanese female, the first case of limited type systemic sclerosis (SSc), developing both NM and MP.
Chika, Ohata   +8 more
openaire   +2 more sources

Solitary morphea profunda following trauma sustained in an automobile accident.

Cutis, 2015
Solitary morphea profunda (SMP) is a variant of localized scleroderma (LS). We report the case of a 50-year-old white woman with a history of trauma sustained in an automobile accident who presented with SMP on the right upper arm. We also provide a review of the classification, epidemiology, etiology, diagnostic studies, pathogenesis, physical ...
Khasha, Touloei   +2 more
openaire   +1 more source

Solitary Morphea Profunda: A Case Report.

Mymensingh medical journal : MMJ
Morphea is an autoimmune connective tissue disease that leads to sclerosis of skin and underlying subcutaneous tissue due to excessive collagen deposition. It is also called localized scleroderma. Morphea profunda is one of the morphological variants of morphea. It involves the deep dermis, subcutaneous tissue, fascia and muscle.
S F, Sobhan   +4 more
openaire   +1 more source

Morphea Profunda

International Journal of Dermatology, 1991
K, Sayama   +3 more
openaire   +2 more sources

Morphea profunda

The American Journal of Dermatopathology, 1981
W P, Su, J R, Person
openaire   +2 more sources

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