Search Results for: wells\\' syndrome

Cutis marmorata telangiectatica congenita restricted to both breasts in a young female

Cutis marmorata telangiectatica congenita restricted to both breasts in a young female

…ns over both breasts where the reticulated pattern and dilated veins are seen. Vascular anomalies, for example, Sturge-Weber syndrome [7], Klippel–Trenaunay–Weber syndrome have been associated with CMTC. The female patient reported in this article…

Eccrine syringofibroadenoma (EFSA): a report of two cases

Eccrine syringofibroadenoma (EFSA): a report of two cases

…with hidrotic ectodermal dysplasia (HED) presents in two different variants, Schöpf-Schulz-Passarge syndrome and Clouston’s syndrome. Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal dominant ectodermal dysplasia, characterized by…

Histologic Diagnosis of Inflammatory Skin Diseases

Subcutaneous T-cell lymphoma

…h cells whose nuclei show prominent abnormalities. Sinus histiocytosis with massive lymphadenopathy (Destombes-Rosai-Dorfman syndrome) is made up of large, pale histiocytes that with immunoperoxidase stain are S-100 positive, and dense, patchy…

Histologic Diagnosis of Inflammatory Skin Diseases

Precepts Adjunctive to the Algorithmic Method

…phocytes and plasma cells and because it reminds by way of analogy (albeit vaguely) of trytophan-myalgia syndrome, toxic oil syndrome, and Shulman’s syndrome, inflammatory conditions all. Last, if a histopathologist is stymied by particular…

Resolving Quandaries in Dermatology, Pathology & Dermatopathology

Discoid Lupus Erythematosus versus Systemic Lupus Erythematosus? II

…panniculitis (LE profundus) 1. With discoid LE 2. With systemic LE II. Subacute cutaneous LE A. Papulosquamous B. Annular C. Syndromes commonly exhibiting similar morphology 1. Neonatal LE 2. Complement deficiency syndrome III. Acute cutaneous LE…

Histologic Diagnosis of Inflammatory Skin Diseases

Histiocytosis X

…nidentified group of cases described as defects in membranous bones, exophthalmos, and diabetes insipidus (Christian’s syndrome). Arch Intern Med 1928;42:611. Rowland RS. Christian’s syndrome and lipoid cell hyperplasias of the…

Resolving Quandaries in Dermatology, Pathology & Dermatopathology

Angiolymphoid Hyperplasia with Eosinophilia/Kimura’s Disease?

…ere are more similarities than differences between subcutaneous angiolymphoid hyperplasia and Kimura’s disease.” Wells GC, Whimster IW. Subcutaneous angiolymphoid hyperplasia with eosinophilia. Br J Dermatol 1969;81:1–15….