Results 31 to 40 of about 13,735 (206)

Acanthosis nigricans in insulinoma

Indian Journal of Endocrinology and Metabolism, 2014
Viveka P Jyotsna, Nishant Raizada, Semanti Chakraborty, S Pal   +3 more
doaj   +3 more sources

Acantose nigricante e cancro gástrico.

Acta Médica Portuguesa, 1989
A case of a 44 years old patient with inoperable gastric adenocarcinoma and exuberant lesions of Acanthosis Nigricans is described. He died nine months after the diagnosis, having experienced disappearance of the cutaneous manifestations after the ...
J A Sarmento, C Rosário, C Santos, S Allegro, A Massa, P Roquete   +5 more
doaj   +1 more source

Rabson-mendenhall syndrome

Indian Journal of Dermatology, 2014
Rabson-Mendenhall syndrome (RMS) is a rare genetic disorder characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, dysplastic dentition, coarse facial features, abnormal glucose ...
Iffat Hassan, Hinah Altaf, Atiya Yaseen
doaj   +1 more source

Diffuse Esophageal Squamous Papillomatosis: A Rare Disease Associated with Acanthosis Nigricans and Tripe Palms

Case Reports in Gastroenterology, 2020
Acanthosis nigricans with tripe palms is one of the skin manifestations of systemic conditions, as well as internal malignancy. There have been reports of this paraneoplastic condition’s association with orocutaneous papillomatosis, but investigations ...
Tanyaporn Chantarojanasiri, Arunluk Buranathawornsom, Apichet Sirinawasatien   +2 more
doaj   +1 more source

A case of acanthosis nigricans coexisting with mycosis fungoides [PDF]

, 2015
Acanthosis nigricans maligna (ANM) is a paraneoplastic phenomenon most commonly associated with visceral adenocarcinoma, in particular, gastric adenocarcinoma.
Cheng, Esther, Magro, Cynthia M, Roy, David B, Esther Cheng, Cheng, Esther ; Roy, David B ; Magro, Cynthia M, David B Roy, Cynthia M Magro   +6 more
core   +1 more source

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa, Joana Rosa Marques Prota, Antonia Paula Marques‐de‐Faria, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Correlation of acanthosis nigricans with insulin resistance, anthropometric, and other metabolic parameters in diabetic Indians

Indian Journal of Endocrinology and Metabolism, 2012
Introduction: Acanthosis nigricans is a non-specific reaction pattern that may accompany obesity, diabetes, excess corticosteroids, pineal tumors, malignancies, and other endocrine disorders.
P P Patidar, P Ramachandra, R Philip, S Saran, P Agarwal, M Gutch, K K Gupta   +6 more
doaj   +1 more source

Acanthosis nigricans: To be or not to be afraid (Review)

Oncology Letters, 2018
Acanthosis nigricans (AN), a skin disorder with high prevalence, represents a dermatological condition with esthetic implications, but otherwise mild symptoms. For any clinician, it is in fact the tip of the iceberg, leading him/her to investigate what lies beneath the surface, since AN points to a systemic problem or disease: metabolic disorder (most ...
Popa, Maria-Linda, Popa, Adrian Claudiu, Tanase, Cristiana, Gheorghisan-Galateanu, Ancuta-Augustina   +3 more
openaire   +3 more sources

A rare diagnosis during evaluation for metabolic dysfunction associated steatotic liver disease: Glycogen storage disease type Ia presenting during adolescence in a male with severe obesity

JPGN Reports, EarlyView.
Abstract Metabolic dysfunction‐associated steatotic liver disease (MASLD) is a common comorbidity of pediatric obesity that predisposes patients to hepatocellular adenomas (HCAs). HCAs however are nonspecific to MASLD and warrant further evaluation. We present a case of a 16‐year‐old male with severe obesity, and persistently elevated liver enzymes ...
Carolena Trocchia, Rachel Herdes, Jodi Gedallovich, Amrita Narang   +3 more
wiley   +1 more source

Childhood acanthosis nigricans

Indian Journal of Paediatric Dermatology, 2019
Acanthosis nigricans (AN) is a frequently encountered dermatological condition seen commonly in middle aged or elderly, but in the recent times, there has been an increase in the childhood cases, especially in the adolescent age group.
Anupam Das, Priyankar Misra, Saumya Panda   +2 more
doaj   +1 more source