Literature DB >> 23226673

Atypical presentation of acanthosis nigricans.

Nirmalya Roy1, Tanima Das, Arup K Kundu, Anupam Maity.   

Abstract

Entities:  

Year:  2012        PMID: 23226673      PMCID: PMC3510947          DOI: 10.4103/2230-8210.103048

Source DB:  PubMed          Journal:  Indian J Endocrinol Metab        ISSN: 2230-9500


× No keyword cloud information.
Sir, We document one case of acanthosis nigricans (AN) in an atypical site. The patient was a 48-year-old achondroplastic, diabetic male, school teacher by profession with a body mass index (BMI) of 26 kg/m2. His clinical examination revealed AN over the nape of the neck, axilla, and forehead [Figure 1]. He had normal developmental milestones, and other systemic examinations were essentially within normal limits. Laboratory investigations revealed glycosylated hemoglobin of 8.6% and dyslipidemia (total cholesterol level of 375 mg/dl, low density lipoprotein level of 195 mg/dl, triglyceride level of 180 mg/dl, and high density lipoprotein level of 36 mg/dl). There was no evidence of internal malignancy in chest radiography, abdominal ultrasound, upper gastrointestinal endoscopy, and colonoscopy.
Figure 1

Acanthosis nigricans seen on forehead

Acanthosis nigricans seen on forehead AN is a brown-to-black velvety hyperpigmentation of skin. The common sites involved are posterior and lateral folds of neck, axilla, umbilicus, and groin.[1] Forehead, oral mucosa, and eyelids are rarely involved. It may be mistaken with giant melanocytic nevus, atrophic seborrheic dermatitis, hemochromatosis, or atopic dermatitis. AN is associated with insulin resistance states like type 2 diabetes, polycystic ovarian syndrome, and obesity. Crouzon's syndrome and Costello's syndrome are also associated with AN. Severe achondroplasia with developmental delays and AN (SADDAN) have been documented.[2] As in our case, achondroplasia without the presence of developmental delays and AN have also been reported. AN is a paraneoplastic manifestation of internal malignancies of stomach, gut, ovary, prostate, and others. AN is a clinical diagnosis only rarely requiring a skin biopsy. However, a meticulous search for underlying disease and malignancy is required. Treatment of AN involves treatment of the underlying disease or tumor, avoidance of precipitating drugs like niacin, steroids, protease inhibitors, and use of topical keratinolytics, oral isotretinoin, metformin, and ultimately, cosmetic surgery.[3]
  3 in total

1.  Acanthosis nigricans revisited.

Authors:  A K Kundu
Journal:  J Assoc Physicians India       Date:  2001-10

Review 2.  The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Authors:  Z Vajo; C A Francomano; D J Wilkin
Journal:  Endocr Rev       Date:  2000-02       Impact factor: 19.871

3.  Improvement of acanthosis nigricans on isotretinoin and metformin.

Authors:  Hobart W Walling; Michael Messingham; Laura M Myers; Camille L Mason; John S Strauss
Journal:  J Drugs Dermatol       Date:  2003-12       Impact factor: 2.114

  3 in total
  2 in total

1.  Acanthosis nigricans in insulinoma.

Authors:  Viveka P Jyotsna; Nishant Raizada; Semanti Chakraborty; S Pal
Journal:  Indian J Endocrinol Metab       Date:  2014-09

Review 2.  An approach to acanthosis nigricans.

Authors:  Meghana Madhukar Phiske
Journal:  Indian Dermatol Online J       Date:  2014-07
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.