Book Chapter10.1016/B978-0-7020-3485-5.00019-X
18 – Metabolic and storage diseases
David Weedon
- 01 Jan 2010
pp 481-500
6
About: The article was published on 01 Jan 2010.
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Cutaneous Manifestations of Internal Malignancy and Paraneoplastic Syndromes
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Atlas of dermatology in internal medicine
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References
Management difficulties due to concurrent dermatitis herpetiformis and variegate porphyria.
S. Varma,S.W. Lanigan +1 more
TL;DR: Although epidermal grafting appears to be an effective and safe method for the treatment of vitiligo, various complications have been reported, of which some are associated with the application of liquid nitrogen, such as postinflammatory hyperpigmentation, hypertrophic scarring, peripheral hypopigmentation and uneven pigmentation.
8
Treatment of porphyria cutanea tarda with phlebotomy in a patient on peritoneal dialysis
TL;DR: This patient is the first reported case, to the authors' knowledge, of a patient with end-stage renal disease with negative hepatitis serology who was not receiving a hepatotoxic drug, or on hemodialysis, who had PCT develop while receiving peritoneal dialysis.
8
Niemann-Pick disease: report of a case with skin involvement.
TL;DR: The case of a 10-month-old female infant with Niemann-Pick disease who was found to have a unique skin lesion, involving both cheeks, is reported, believed to be the first time that unequivocal involvement of the skin by NiemANN- pick disease has been demonstrated.
7
Porphyria cutanea tarda with menopausal exacerbation: the possible role of menstruation as natural phlebotomy.
Eri Nishioka,Yoko Funasaka,Toshinori Bito,Akira Ito,Masahiro Tani,Akira Kawara,Seitetsu Yoon,Masao Kondo,Masamitsu Ichihashi +8 more
TL;DR: A 48-year-old woman with a 12-year history of porphyria cutanea tarda who showed a remarkable exacerbation of her eruptions accompanied by high serum levels of iron and ferritin at menopause is described.
7
Reactions to light on the normal and pellagrous Bantu skin.
TL;DR: In dark skinned subjects, delayed or “secondary” pigmentation from ultra‐violet light may be the only clinical sign of sunburn and the hyperkeratotic pellagrous lesion is interpreted as a marked reaction to mild or repeated ultraviolet injury followed by retention and ultimate cracking of the abnormal layers so produced.
7
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