Oral stanozolol in lichen sclerosus et atrophicus.

J Am Acad Dermatol

Himalayan Institute of Medical Sciences, Jolly Grant, Dehradun, U.P., India.

Published: February 1998

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0190-9622(98)70251-8DOI Listing

Publication Analysis

Top Keywords

oral stanozolol
4
stanozolol lichen
4
lichen sclerosus
4
sclerosus atrophicus
4
oral
1
lichen
1
sclerosus
1
atrophicus
1

Similar Publications

Article Synopsis
  • Stanozolol is a synthetic anabolic steroid used by bodybuilders to increase muscle mass, but it can cause severe liver damage, including fatal conditions like hepatic necrosis.
  • A case report details the death of a 35-year-old bodybuilder who developed jaundice and liver failure after three months of stanozolol use, confirming the drug's presence in his system during autopsy.
  • The death was attributed to liver injury caused by stanozolol overdose, highlighting the urgent need for increased awareness about the risks of anabolic steroid use, especially with its rising popularity.
View Article and Find Full Text PDF

Background: Giant cellulitis-like Sweet syndrome (SS) is a rare subtype of SS, and reports of the combined histiocytoid type of pathology are scarce. Here, we report a case of SS with distinctive clinical presentations and which was difficult to distinguish from cellulitis. By sharing this case and a discussion of the related literature in detail, we aim to provide clinicians with new insights into the characteristics of histiocytoid giant cellulitis-like (HGC)-SS and the pathogenesis of SS.

View Article and Find Full Text PDF

A fundamental challenge in preventive doping research is the study of metabolic pathways of substances banned in sport. However, the pharmacological predictions obtained by conventional in vitro or in vivo animal studies are occasionally of limited transferability to humans according to an inability of in vitro models to mimic higher order system physiology or due to various species-specific differences using animal models. A more recently established technology for simulating human physiology is the "organ-on-a-chip" principle.

View Article and Find Full Text PDF

Background: Hereditary angioedema (HAE) is a rare inherited disorder characterized by sudden and unpredictable appearance of swelling. Surgical procedures, even minor ones, are known to precipitate an attack in these patients. C1 esterase inhibitor (C1-INH) therapy may be effective for short term prophylaxis in such situations.

View Article and Find Full Text PDF

Compression therapy is the gold standard treatment for venous leg ulcers (VLUs); however, with adjunctive pharmacological therapies and poor patient adherence using compressive dressings, clinicians are looking to find the advantage in treating VLUs. This literature review focuses on the efficacy of pharmacological agents, quality of life using agents in addition to compression therapy, and cost effectiveness to indicate the best outcomes for pharmacological treatment of VLUs. The following available venotonic, hemorheologic, and fibrinolytic agents were reviewed for oral management in treating VLUs: pentoxifylline, flavonoids (diosmin, hidrosmin, rutosides, and micronized purified flavonoid fraction, Vasculera), Red-Vine-Leaf-Extract AS 195, Ruscus, Ginkgo biloba, Centella asiatica, Pycnogenol (French maritime pine bark), escin/horse chestnut extract, nutritional supplements (ie, zinc and magnesium, glycosaminoglycans [sulodexide], mesoglycans), Axaven, cilostazol, fibrinolytic enhancers (stanozolol and defibrotide), calcium dobesilate, aspirin, antibiotics (antimicrobials, doxycycline, levamisole), diuretics, cinnarizine, naftazone, and benzarone.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!