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1.
Z Hautkr ; 61(24): 1793-8, 1986 Dec 15.
Artigo em Alemão | MEDLINE | ID: mdl-3825220

RESUMO

We report on 3 families showing increased occurrence of malignant melanoma (MM). As the patients suffering from MM also revealed great numbers of nevi, we suspected dysplastic naevus syndrome.


Assuntos
Síndrome do Nevo Displásico/genética , Melanoma/genética , Neoplasias Cutâneas/genética , Adulto , Feminino , Antígenos HLA/genética , Haplótipos , Humanos , Masculino
2.
Dermatologica ; 163(1): 19-24, 1981.
Artigo em Inglês | MEDLINE | ID: mdl-7274513

RESUMO

A patient suffering from an advanced and inoperable gastric carcinoma developed an unusual paraneoplastic syndrome, consisting of intensive pruritus, acanthosis nigricans, sign of Leser-Trélat (seborrhoic keratoses and freckles), warty and papillomatous excrescences, palmoplantar hyperkeratosis and florid papillomatous and granular lesions of the mouth mucosa. The whole skin of the patient was involved. The authors believe this disorder to be generalized acanthosis nigricans. As a cause they suggest the possibility of a growth-stimulating factor, produced by the tumor cells. The relationship of acanthosis nigricans with the sign of Leser-Trélat is discussed.


Assuntos
Acantose Nigricans/etiologia , Síndromes Paraneoplásicas/diagnóstico , Neoplasias Gástricas/complicações , Acantose Nigricans/diagnóstico , Substâncias de Crescimento/metabolismo , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Gástricas/metabolismo
3.
Br J Dermatol ; 101(3): 345-50, 1979 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-508599

RESUMO

Cutis marmorata telangiectatica congenita was observed in two adult sisters. The condition appeared at birth and did not change much with age. In one sister the condition was accompanied by hypertension, acrocyanosis and ulceration of the big toe. On the basis of a comparison of the symptoms in patients and their relatives, the authors assume that Van Lohuizen syndrome is a dominantly inherited genetic disorder with low penetrance and great intrafamilial variability.


Assuntos
Dermatopatias/congênito , Telangiectasia/congênito , Adulto , Feminino , Humanos , Linhagem , Dermatopatias/complicações , Dermatopatias/genética , Síndrome , Telangiectasia/complicações , Telangiectasia/genética
4.
Arch Dermatol ; 115(6): 761, 1979 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-453885
5.
Hautarzt ; 29(4): 219-21, 1978 Apr.
Artigo em Alemão | MEDLINE | ID: mdl-148438

RESUMO

A patient with hyperkeratotic and vegetating mycosis fungoides is reported. The immunologic investigations reveal a well preserved immunologic response. The clinical manifestations are considered as an hyperergic reaction of a sentizied organism.


Assuntos
Micose Fungoide/diagnóstico , Adulto , Reações Antígeno-Anticorpo , Dermatite Esfoliativa/diagnóstico , Diagnóstico Diferencial , Feminino , Humanos , Ceratodermia Palmar e Plantar/diagnóstico , Doenças Linfáticas/diagnóstico , Micose Fungoide/imunologia , Síndrome
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