ABSTRACT
An up-to-date overview of antithrombotic drugs, with their currently reported beneficial cutaneous effects and skin side effect, is presented. Attempts to balance traditional pharmacodynamic concepts with the newly described empiric benefits are made. A concise, current and useful reference for dermatologists with an interest in dermatopharmacology and the practicing physician in the field of wound care, vasculitides and skin involvement of internal diseases is tried to be achieved
Subject(s)
Humans , Fibrinolytic Agents/adverse effects , Dipyridamole/adverse effects , Pentoxifylline/adverse effects , Pentoxifylline/pharmacology , Ticlopidine/pharmacology , Ticlopidine/adverse effects , Aspirin/pharmacology , Dipyridamole/pharmacology , Aspirin/adverse effectsSubject(s)
Humans , Skin Diseases , Anesthesia, Local/adverse effects , Anesthesia/adverse effects , DermatologyABSTRACT
Subcutaneous fat necrosis [SCFN] occurs in term newborn with history of difficult delivery. Apart from the soft tissue lesions, the infants may suffer from life threatening hypercalcemia as a complication of disease requiring various medications. A case of subcutaneous fat necrosis with history of birth asphyxia is presented and clinical course and treatment options are discussed
Subject(s)
Humans , Female , Fat Necrosis/pathology , Infant, Newborn , Asphyxia NeonatorumABSTRACT
Dermatopathology still remains the fundament of the entire dermatology study. Different approaches have been implicated to facilitate the diagnostic process in dermatopathology. To date, many specific dermatopathological findings have been introduced to indicate a particular disease. Most of them however can not fulfill the criteria of applicability and good clinico-pathological correlation. Herein we take the challenge of promoting a useful catalogue of the most common terms used by dermatopathologists
Subject(s)
Humans , Skin Diseases/diagnosis , DermatologyABSTRACT
Hereditary Hypotrichosis Simplex of the Scalp [HHSS] is a relatively rare form of hereditary alopecia. Herein, we report 2 additional families affected with this disorder
Subject(s)
Humans , Female , Hypotrichosis/genetics , Scalp Dermatoses , Genetic Diseases, InbornABSTRACT
We report an 11-year-old girl with well defined ichthyosiform patches on extremities. There is a history of similar condition in her cousin. We believe that this case represent a new autosomal recessive disorder of cornification that may be better refer to it as "progressive symmetric exfoliative ichthyosis"
Subject(s)
Humans , Female , Ichthyosis/pathologyABSTRACT
Genodermatoses in the Gulf countries have been re- viewed. The high occurrence of diseases like epidermolysis bullosa, mal de Meleda and biotinidase deficiency have been noted. New syndromes are also continuously being reported. Molecular studies have revealed findings different from those described elsewhere. These have been linked to the large family size and tribal customs that lead to consanguinity. Influx of immigrants, wars and environmental pollutants are likely to worsen the situation. As treatment of genetic disorders is a challenging issue, prevention must be targeted by providing good premarital counseling and altering the tribal customs that promote consanguinity