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1.
An. bras. dermatol ; 89(2): 361-362, Mar-Apr/2014. graf
Article Dans Anglais | LILACS | ID: lil-706980

Résumé

Multiple autoimmune syndrome is a rare condition, described by Humbert and Dupond in 1988. It is defined by the association of at least 3 autoimmune diseases in the same patient. Vitiligo is the most common skin condition in this syndrome. This article presents the case of a 31-year-old male with vitiligo, alopecia areata, Crohn's disease, psoriasis vulgaris and oral lichen planus. The rarity of this case is highlighted by the coexistence of four autoimmune skin diseases in association with Crohn's disease, never described in the literature.


Sujets)
Humains , Mâle , Adulte , Psoriasis/anatomopathologie , Maladies auto-immunes/anatomopathologie , Vitiligo/anatomopathologie , Maladie de Crohn/anatomopathologie , Lichen plan buccal/anatomopathologie , Pelade/anatomopathologie , Psoriasis/complications , Maladies auto-immunes/complications , Syndrome , Vitiligo/complications , Maladie de Crohn/complications , Lichen plan buccal/complications , Pelade/complications
2.
An. bras. dermatol ; 89(1): 173-174, Jan-Feb/2014. graf
Article Dans Anglais | LILACS | ID: lil-703537

Résumé

Cutaneous involvement associated to multiple myeloma varies from 5 to 10% of cases and is infrequently recognized. Cutaneous metastatic plasmacitomas are rare. We present the case of a 72-year-old man with multiple myeloma in complete remission since 2 years ago with cutaneous tumors on the trunk and face. A cutaneous biopsy was consistent with plasmacytoma. The patient was treated with melphalan, prednisolone and radiotherapy. Despite optimal therapeutic response of the lesions, the disease progressed, with the appearance of new extra-cutaneous plasmocytomas. The cutaneous metastatic plasmocytomas were the first sign of progression of the disease.


Sujets)
Humains , Mâle , Sujet âgé , Plasmocytome/secondaire , Tumeurs cutanées/secondaire , Myélome multiple/anatomopathologie , Peau/anatomopathologie , Biopsie , Moelle osseuse/anatomopathologie , Immunohistochimie , Évolution de la maladie
3.
An. bras. dermatol ; 88(6,supl.1): 26-28, Nov-Dec/2013. graf
Article Dans Anglais | LILACS | ID: lil-696830

Résumé

The paradoxical adverse effects of tumor necrosis factor-alpha (TNF-alpha) antagonists have been described frequently as a result of the widespread use of these drugs. Among the TNF-alpha blocking agents, few reports exist relating the use of adalimumab in cutaneous sarcoidosis, although all of them show good results. More recently, sarcoidosis onsets have been reported with various TNF-alpha inhibitors. The current case is, to our knowledge, the first to describe the exacerbation of cutaneous lesions of sarcoidosis treated with adalimumab.


Os efeitos paradoxais dos anti-TNF-alpha têm sido cada vez mais descritos com a utilização mais ampla dessas drogas. Entre os TNF-alpha, registam-se poucos casos com a utilização de adalimumab no tratamento da sarcoidose cutânea, sendo que todos eles apresentam bons resultados. Têm sido descritos, mais recentemente, casos de sarcoidose induzidos por vários anti-TNF-alpha. O presente caso é, até à data, o primeiro a descrever a exacerbação de lesões cutâneas de sarcoidose tratadas com adalimumab.


Sujets)
Femelle , Humains , Adulte d'âge moyen , Anti-inflammatoires/effets indésirables , Anticorps monoclonaux humanisés/effets indésirables , Sarcoïdose/traitement médicamenteux , Maladies de la peau/traitement médicamenteux , Facteur de nécrose tumorale alpha/antagonistes et inhibiteurs , Biopsie , Évolution de la maladie , Sarcoïdose/anatomopathologie , Maladies de la peau/anatomopathologie , Résultat thérapeutique
4.
An. bras. dermatol ; 88(6): 1009-1010, Nov-Dec/2013. graf
Article Dans Anglais | LILACS | ID: lil-699012

Résumé

POEMS syndrome is a unique clinical entity, the diagnosis of which is made when polyneuropathy and monoclonal gammopathy occur together, associated with other changes such as organomegaly, endocrinopathy, skin changes and papilledema. Cutaneous manifestations are heterogeneous, with diffuse cutaneous hyperpigmentation, hemangiomas and hypertrichosis occurring more frequently. We report the case of a 65- year-old female patient with this syndrome, diagnosed after 15 years of disabling peripheral neuropathy.


A síndrome de POEMS é uma entidade clínica única cujo diagnóstico é colocado quando existe polineuropatia e gamapatia monoclonal associada a outras alterações tais como organomegalia, endocrinopatia, alterações cutâneas e papiledema. As manifestações cutâneas são heterogéneas, sendo as mais frequentes a hiperpigmentação cutânea difusa, os hemangiomas e a hipertricose. Relata-se o caso de uma doente de 65 anos com essa síndrome diagnosticada após 15 anos de neuropatia periférica.


Sujets)
Adolescent , Femelle , Humains , Hypotrichose/congénital , Dégénérescence maculaire/congénital , Hypotrichose/diagnostic , Dégénérescence maculaire/diagnostic , Syndrome
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