Calcinosis cutis is an uncommon soft tissue lesion characterized by the deposition of calcium salts in skin or subcutaneous attributed to a wide variety causes. We present case idiopathic calcinosis adult male, who presented with swelling right iliac region. Chalky white aspirate and amorphous basophilic granular material on microscopy suggestive deposits were noted. Histopathological examinati...

Cutis laxa, clinically characterized by loose and pendulous skin related to loss of elastic tissue, is a rare heterogeneous condition. It is classified into congenital and acquired types. We report a case of generalized acquired cutis laxa type 1 in a young man following pruritic urticarial plaques. We have done a brief review of literature.

Sir, Lymphocytoma cutis of Spiegler-Fendt type is a rare chronic B lymphocyte proliferation a¡ecting the head and the neck in particular. It is characterized by solitary or grouped nodules or plaques which are purple or red and may reach a diameter of 3 ^ 5 cm. Although lymphocytoma cutis is a benign disorder, it often runs a protracted, even life-long course. Progression to malignant B cell ly...

INTRODUCTION Phacomatosis pigmentovascularis is a rare congenital condition characterized by vascular malformation associated with extensive pigmented nevi. Even though it forms a large, prominent skin lesion, therapy for phacomatosis pigmentovascularis is rarely discussed. To the best of our knowledge, this is the first report of phacomatosis pigmentovascularis type II treated with combined la...

Background: The Pelger-Huet anomaly dominantly is a rare and benign inherited defect of terminal neutrophil differentiation. Although neutrophil migration may be minimally impaired, granulocytes function is otherwise normal association abnormalities such as ocular, musculoskeletal are reported very rare. Case: An eight year-old boy with good consciousness but severe muscular atrophia and diffic...

Aplasia cutis congenita is the congenital absence of skin mostcommonly affecting the scalp. No definite etiology is available butmultiple causes such as intrauterine infection, fetal exposure tococaine, heroin, alcohol or antithyroid drugs, vascular disruption,genetic causes, syndromes and teratogens have been suggested.We present an infant with extensive aplasia cutis of the trunk andthigh. He...

Cutis verticis gyrata is characterized by excessive formation of scalp skin. It may be primary (essential and nonessential) or secondary. In the primary essential form it presents only folding skin formation on the scalp, mimicking cerebral gyri, without associated comorbidities. We report a rare case of a 28 year-old male patient with primary essential cutis verticis gyrata.