Chapter

Chapter-33 Ages of Man and their Dermatoses

January 2015

DOI:10.5005/jp/books/12564_34

In book: A Manual of Dermatology (pp.682-699)

Authors:

Shernaz Walton

National Health Service

ResearchGate has not been able to resolve any citations for this publication.

ResearchGate has not been able to resolve any references for this publication.

Chapter

Autoantikörperdiagnostik

January 1995

Bullöse Autoimmundermatosen, die histologisch durch eine subepidermale Spaltbildung und immunfluoreszenzoptisch durch lineäre Ablagerungen von Immunglobulinen und/oder Komplementkom ponenten charakterisiert sind, umfassen das bullöse Pemphigoid (BP), den Herpes gestationis, das ver narbende Pemphigoid (VP), die Epidermolysis bullosa acquisita (EBA), die lineare IgA-Dermatose und die ... [Show full abstract] chronisch-bullöse Dermatose des Kindesalters. Der Nachweis von Autoantikörpern, die gegen Strukturproteine der dermoepidermalen Basalmembranzone (BMZ) (Anti-BMZ-Autoantikörper) gerichtet sind, gehört heute unabdingbar zum dia gnostischen Profil dieser Erkrankungsgruppe. Bei klinisch typischem Bild und Nachweis der besagten feingeweblichen Merkmale ist bei einem Großteil der Patienten eine genaue Zuordnung möglich. Es können sich allerdings, wie auch von anderen Ar beitsgruppen betont, vor allem beim BP, der EBA und dem VP die klinischen Bilder derart gleichen, daß eine Unterscheidung mit Routineuntersuchun gen nicht möglich ist. In diesen Fällen muß man weitere diagnostische Schritte, die Bezug auf die Lo kalisation der Autoantikörperbindung oder deren Spezifität nehmen, anschließen.

Article

Steatocystoma Multiplex with Pachyonychia Congenita

November 1961 · Archives of Dermatology

William R. Vineyard

Steatocystoma multiplex and pachyonychia congenita are uncommon genodermatoses, judging from the sparcity of reports of either condition in the medical literature.1-6 The observation of a patient in whom both conditions exist and can be traced through 4 generations appears to represent a combination of hereditable dermatoses never before reported. The purpose of this paper is to report 8 cases of ... [Show full abstract] these combined disorders and present the results of dermabrasion therapy in the management of one patient. Report of a Case A 35-year-old white man came to the dermatology clinic complaining of numerous "bumps on his skin and thick nails." He stated the thickened nails were first noted when he was approximately 7 months of age. His skin was essentially clear until he was 20 years old when numerous yellow, elevated nodules developed on his face. These lesions have progressively increased in size and number and have since appeared over

Article

[The man behind the syndrome: Thomas Addison. One of the 3 giants at Guy's Hospital--he introduced s...

June 1988 · Läkartidningen

R Luft

Article

Lupus vulgaris (verrucosus) associated with pulmonary tuberculosis

January 1970

T.R. Kapur

An unusual case of Lupus Vulgaris (Verrucosus) associated with Pulmonary Tuberculosis in a young man is presented. He had asymptomatic pulmonary tuberculosis and developed a cold abscess in the perineum, leading to two bilateral, symmetrical Verrucosus plaques in the Ischiorectal areas. Chemotherapy gave excellent results.

Article

[Man with arterial hypertension, skin lesion and splenic nodules]

November 2008 · Revista Clínica Española

Article

Chronic lichenoid keratosis. Report of two cases

January 2000 · Giornale Italiano di Dermatologia e Venereologia

Two cases of chronic lichenoid keratosis (clk) in two blake patients are reported. The former case concerns a man who was born in 1959. He came to Italy in 1986. The dermatosis manifested itself through keratotic papules and multiple black-bluish nodules. These lesions showed themselves as developing poussees which spread outwards from the trunk, into the limbs in the palms and on the face; ... [Show full abstract] psoriasiform lesions were present on the palms and soles. Findings of a biopsy specimen proved it to be characteristic of clk. The latter case concerns a man who was born in 1953 who had been in Italy since 1990 and HIV-positive since 1993. The patient showed keratotic papular-nodular lesions on the trunk and, afterwards on the limbs. Psoriasiform lesions were present on the palms and soles. The biopsy of the papula was compatible with clk. The occurrence of clk associated with AIDS has not previously been reported. This clinical entity was described for the first time by Kaposi in 1895. It was considered as a variant of lichen ruber planus. This dermatosis is very rare, chronic and progressive. It has unknown etiology and it is difficult to classify nosologically.

Article

Cancer in Man at Site of Prior Benign Lesion of Skin or Mucous Membrane: A Review

August 1972 · Cancer Research

Lucia J. Dunham

SUMMARY

Article

Ofuji's papuloerythroderma. An association with early gastric cancer

July 1999 · European journal of dermatology: EJD

A case of Ofuji's papuloerythroderma in an 88-old man, affected by early gastric cancer, is reported. The association noticed in our case with early visceral malignancy is the starting point for the consideration of pathological relationships, nosological and prognostic evaluations in regard to this rare dermatosis which is distinctive of elderly people, and underlines the importance of a ... [Show full abstract] long-term follow-up of these patients.

Article

Persistent acantholytic dermatosis: Sex-related differences in clinical presentation?

March 1993 · Acta Dermato-Venereologica

We report the case of a 58-year-old man with a chronic papular eruption of 10 years' duration. Histopathology revealed focal acantholytic dyskeratosis. This condition is thought to represent a distinct entity which has been reported under several names and frequently referred to as persistent acantholytic dermatosis. The relationship between this condition and transient acantholytic dermatosis ... [Show full abstract] (Grover's disease), emphasizing sex-related presentations, is discussed.

Article

Chronic atrophic erosive dermatosis of the scalp and atypical fibroxanthoma: A rare association

May 2012 · European journal of dermatology: EJD

ejd.2012.1767 Auteur(s) : Francesco Savoia1,2 francesco.savoia@ausl.ra.it, Caterina Stinchi1, Lorenzo Valenti1, Laura Baldassari1, Giuseppe Gaddoni1, Federica Giacomini2, Annalisa Patrizi2, Loredana Cardinale3, Silvia Zago3 1 Unit of Dermatology, 2 Department of Internal Medicine Division of Dermatology, University of Bologna, Italy 3 Unit of Pathologic Anatomy, AUSL Ravenna, viale Dante 10, ... [Show full abstract] 48022 Lugo, Ravenna, Italy A 77-year-old Caucasian man, with a 10-year history of actinic keratoses treated [...]

Article

Cutaneous arteritis with superior vena cava obstruction

May 1979 · British Journal of Dermatology

Superior vena cava (SVC) obstruction may occur in several disorders (Urschel & Paulson, 1966) and may be associated with arteritis in Behçet's disease (Chajek & Farinaru, 1975). We report a man who had arteritis and SVC obstruction without any of the known causes.

Article

Dermatophilus Infection in Animals and Man

December 1976 · Journal of Investigative Dermatology

Nardo Zaias

Chapter-33 Ages of Man and their Dermatoses

No full-text available

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