Results 71 to 80 of about 207 (118)
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Postvaccination Morphea Profunda in a Child
Pediatric Dermatology, 2011Abstract: We report a new case of postvaccination morphea profunda (MP) in a child and discuss its different clinical presentations, prognosis, and therapy and its relationship with “solitary morphea profunda.” A 2‐year‐old healthy girl presented with an induration of the anterior aspect of the left thigh of 9 months duration.
Aida, Khaled +6 more
openaire +2 more sources
Nishi Nihon Hifuka, 2006
症例は60歳の男性。10年前より尋常性乾癬を加療中。約半年前より，右前腕の屈側尺側に皮下硬結としびれが出現し，徐々に悪化した。皮膚の表面は常色で境界は不明瞭。Raynaud現象及び，強指症は認めなかった。激しい運動，有機溶剤の暴露，L-トリプトファンの摂取歴はなかった。病理組織では脂肪織隔壁，筋膜の硬化性変化と著明な肥厚を認めた。組織および末梢血の好酸球の増多はなかった。血清中抗核抗体は80倍陽性であった。Morphea profundaと診断した。ステロイド内服はせず経過観察中であるが，皮下硬結の拡大はない。
Takehiko MIYAKAWA +3 more
openaire +1 more source
症例は60歳の男性。10年前より尋常性乾癬を加療中。約半年前より，右前腕の屈側尺側に皮下硬結としびれが出現し，徐々に悪化した。皮膚の表面は常色で境界は不明瞭。Raynaud現象及び，強指症は認めなかった。激しい運動，有機溶剤の暴露，L-トリプトファンの摂取歴はなかった。病理組織では脂肪織隔壁，筋膜の硬化性変化と著明な肥厚を認めた。組織および末梢血の好酸球の増多はなかった。血清中抗核抗体は80倍陽性であった。Morphea profundaと診断した。ステロイド内服はせず経過観察中であるが，皮下硬結の拡大はない。
Takehiko MIYAKAWA +3 more
openaire +1 more source
Eosinophils in lupus panniculitis and morphea profunda
Journal of Cutaneous Pathology, 1991The extent of eosinophils in skin biopsy and peripheral blood specimens of patients with lupus panniculitis and morphea profunda was determined by studying 37 biopsies from 33 patients with lupus panniculitis and 55 biopsies from 53 patients with morphea profunda. Specimens from 8 (24%) of 33 patients with lupus panniculitis showed eosinophils, and 13 (
M S, Peters, W P, Su
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Cutaneous lupus erythematosus, morphea profunda and psoriasis: A case report
Reumatología Clínica (English Edition), 2020Psoriasis is a common inflammatory dermatosis that may be associated with a number of diseases. Recent studies provide evidence that there is a greater frequency of autoimmune diseases, but association with autoimmune connective tissue diseases is uncommon. The coexistence of psoriasis and lupus erythematosus is rare. Besides, the occurrence of morphea
Mónica, García-Arpa +5 more
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‘Swiss Cheese’ Lymphangiectasia in a Case of Solitary Morphea Profunda
The Journal of Dermatology, 1997AbstractReports of lymphangiectases that occur in lesions of morphea are rare. We describe a 24‐year‐old woman with a solitary morphea profunda associated with lymphangiectasia. Unlike previously reported cases, our case showed lymphatic dilatation resembling Swiss cheese and developed around a milium.
S K, Ahn +5 more
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Periodic Follow‐Up Is Necessary in Morphea Profunda to Identify Systemic Evolution
SKINmed: Dermatology for the Clinician, 2005The term “morphea” includes a wide spectrum of clinical entities, varying from localized plaques of only cosmetic importance to deep lesions resulting in considerable morbidity for the patient. In fact, although survival rates are no different from that of the general population, localized scleroderma May be associated with development of substantial ...
Lucilla Melani +5 more
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Facial solitary morphea profunda presenting with painful trigeminal neuropathy: A case report
Cephalalgia, 2018Background Localized facial scleroderma usually presents as frontal linear morphea or progressive hemifacial atrophy. Only isolated cases of trigeminal painful neuropathy have been described. Case report A 43-year-old woman developed an oval lesion on the right cheek.
David Moreno-Ajona +4 more
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Ultrasonography as an auxiliary diagnostic tool for morphea profunda: A case report
The Journal of Dermatology, 2019AbstractMorphea profunda is a rare subtype of localized scleroderma and it is difficult to evaluate the conditions of sclerotic changes at an early stage. Studies using ultrasonography to evaluate localized scleroderma are limited and, to date, the characteristic findings of morphea profunda assessed by ultrasonography have never been reported.
Minghsiu Hsieh +5 more
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Plasma cell panniculitis, a type of morphea profunda, surrounded by congenital nevus spilus
European Journal of Dermatology, 2016Plasma cell panniculitis (PCP), a rare histopathological subtype of morphea profunda, demonstrates local sclerosis associated with abundant plasma cell infiltrates [1]. Only seven cases of PCP have been reported in PubMed [1-5]. Here we report a case of PCP surrounded by nevus spilus and we review previous reports.A 33-year-old female presented with an
Chihiro, Shiiya +5 more
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Annals of the Rheumatic Diseases, 2015
Background Deep Variant Morphea (DMV), previously known as morphea profunda, is an exceptionally rare form of sclerosis that is confined to the skin, and unlike scleroderma, has no systemic or internal organ involvement. The inflammation and sclerosis involves layers of the deep dermis, panniculus, fascia or even the underlying superficial muscle.
F. Adeeb +7 more
openaire +1 more source
Background Deep Variant Morphea (DMV), previously known as morphea profunda, is an exceptionally rare form of sclerosis that is confined to the skin, and unlike scleroderma, has no systemic or internal organ involvement. The inflammation and sclerosis involves layers of the deep dermis, panniculus, fascia or even the underlying superficial muscle.
F. Adeeb +7 more
openaire +1 more source