نتایج جستجو برای: malignant acanthosis nigricans

تعداد نتایج: 212845  

Journal: :journal of skin and stem cell 0
vishalakshi s. pandit department of dermatology, hospital and research centre, venereology and leprosy, sbmp medical college, blde university, bijapur, india; department of dermatology, hospital and research centre, venereology and leprosy, sbmp medical college, blde university, p. o. box: 586103, bijapur, india. tel: +91-9844381033 arun c. inamadar department of dermatology, hospital and research centre, venereology and leprosy, sbmp medical college, blde university, bijapur, india aparna palit department of dermatology, hospital and research centre, venereology and leprosy, sbmp medical college, blde university, bijapur, india

conclusions metabolic abnormalities in bscl may prove fatal necessitating optimal therapeutic and preventive measures. patients are advised low fat diet with enhanced physical activities. other treatments include metformin, n-3 polyunsaturated fatty acids and leptin replacement for correction of metabolic complications. we report this case of bscl in view of its rarity. case presentation an 18 ...

2017
Jacqueline Deen Thomas Moloney David Burdon-Jones

Acanthosis nigricans (AN) is a dermatopathy associated with insulin-resistance, drugs, endocrine disorders, chromosomal abnormalities (benign AN), and neoplasia (malignant AN). Malignant AN (MAN) is a rare paraneoplastic skin syndrome most commonly associated with gastric adenocarcinoma and other intra-abdominal malignancies. We report the case of a 28-year-old female with AN associated with ob...

Journal: :Indian journal of cancer 2008
R Mongha S Narayan Rk Das Ak Kundu

Sir, Paraneoplastic syndromes are defined as nonmetastatic systemic effects that accompany malignant disease. These syndromes may occur in up to 10-15% of malignancies. A few paraneoplastic syndromes have been reported in metastatic transitional cell carcinoma including hypercalcemia, thrombocytosis, eosinophilia, nephrotic syndrome, acanthosis nigricans, dermatomyositis, polymyositis, and leuk...

Journal: :Proceedings of the Royal Society of Medicine 1932

Journal: :QJM : monthly journal of the Association of Physicians 2008
S Ghosh B Roychowdhury S Mukhopadhyay S Chowdhury

Acanthosis nigricans is said to be a marker of insulin resistance. It is known to occur in patients with insulinoma where there is marked hyperinsulinaemia. We report a case wherein the acanthosis disappeared following surgical resection of insulinoma and this strengthens the hypothesis that hyperinsulinaemia is responsible for acanthosis.

Journal: :TheScientificWorldJournal 2006
Kristin M Rager Hatim A Omar

HAIR-AN syndrome (hyperandrogenism, insulin resistance, acanthosis nigricans) is a subset of the polycystic ovary syndrome, where the patients demonstrate severe insulin resistance. It is theorized that both genetic and environmental factors, such as obesity, give rise to the development of HAIR-AN. Diagnosis is primarily clinical, with laboratory values lending further support. Treatment is ai...

Journal: :Postgraduate medical journal 1990
G S Conway H S Jacobs

Fasting and stimulated insulin concentrations in four patients with acanthosis nigricans and polycystic ovary syndrome were compared with four patients, matched for weight and ovarian morphology, without acanthosis. The median fasting serum insulin concentrations were 114.2 and 25.1 mU/l in the respective groups (P = 0.02). One additional patient was investigated before and after an 18% increas...

Journal: :American family physician 2001
K B Elmer R M George

HAIR-AN syndrome is an acronym for an unusual multisystem disorder in women that consists of hyperandrogenism (HA), insulin resistance (IR) and acanthosis nigricans (AN). The precipitating abnormality is thought to be insulin resistance, with a secondary increase in insulin levels and subsequent overproduction of androgens in the ovaries. Long periods of hyperinsulinism and, some suspect, hyper...

Journal: :Dermatology online journal 2010
Anne C de Waal Michelle M van Rossum H Jorn Bovenschen

Eight cases of the acanthosis nigricans form of epidermal nevus have been described in literature. The present case is impressive and has an extensive segmental distribution. Although etiological factors, such as mutations in the FGFR3 gene, are becoming recognized, treatment options remain limited. We present a case of a 14-year-old male with multiple hyperpigmented, hyperkeratotic plaques on ...

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