Results 51 to 60 of about 369,222 (166)

Oral malignant acanthosis nigricans associated with serous endometrial carcinoma: a case report and review of the literature

open access: yes, 2021
Malignant acanthosis nigricans is a paraneoplastic cutaneous syndrome. Clinical findings such as tripe palms and mucocutaneous papillomatosis in atypical sites such as the oral mucosa are strong indicators of a visceral malignancy.
Bayramgurler, D., Ozden, H. K.
core  

Acanthosis nigricans: An extensive review

open access: yes, 2021
Acanthosis nigricans (AN) is a velvety, hyperpigmentation of the skin that usually occurs in intertriginous areas. AN is most commonly associated with benign disorders like diabetes, insulin resistance, endocrinopathies and exogenous medications, but can
Sajad Ahmad Salati   +2 more
core   +1 more source

Cutaneous clues: Malignant acanthosis nigricans and tripe palms as first signs of recurrent endometrial carcinoma

open access: yesTaiwanese Journal of Obstetrics & Gynecology
Objective: ‘Tripe palm’ is a rare cutaneous paraneoplastic syndrome characterized by velvety thickening of the palms with a ridged or rugose appearance. The condition, either on its own or in combination with acanthosis nigricans, is strongly associated ...
Da-Hsin Dzwo   +4 more
doaj   +1 more source

Generalized benign acanthosis nigricans in an infant

open access: yes, 2014
The generalized form of acanthosis nigricans, especially in infants, is extremely rare. Herein we report a 1-year-old female child who developed generalized acanthosis nigricans without any evidence of internal malignancy or endocrine disorder. This case
Dhiraj Kumar   +3 more
core   +1 more source

Head and Neck Clinical Signs Associated With Diseases: A Scoping Review

open access: yesSpecial Care in Dentistry, Volume 46, Issue 3, May/June 2026.
ABSTRACT Objective Clinical signs observed during head and neck examination offer important diagnostic clues. This scoping review aimed to identify key clinical signs in this region associated with diseases and syndromes and to map them according to their location. Methods An electronic literature search was performed in five databases (Embase, LILACS,
Helena Miguel Cotter   +8 more
wiley   +1 more source

Case Report Acanthosis Nigricans Associated with an Adrenocortical Tumor in a Pediatric Patient [PDF]

open access: yes, 2020
Malignant acanthosis nigricans (AN) is a rare paraneoplastic syndrome seen primarily in adults with an underlying diagnosis of gastrointestinal adenocarcinoma.
N Demura   +9 more
core  

MİDE ADENOKARSİNOMLU BİR HASTADA AKANTOZİS NİGRİKANS

open access: yesCerrahpaşa Medical Journal, 2014
Background and Design.- Acanthosis nigricans is classified into benign and malignant forms on the basis of clinical associations. Most importantly, it often precedes the diagnosis of a new or recurrent tumor.
Özlem AKÇA   +5 more
doaj  

Florid Cutaneous Papillomatosis, Malignant Acanthosis Nigricans, and Pulmonary Squamous Cell Carcinoma

open access: yes, 1991
: A 72‐year‐old man had florid cutaneous papillomatosis (FCP), which is an obligatory paraneoplastic syndrome always associated with an internal malignancy. The cancer, which is usually intraabdominal and most often gastric in origin, evolves parallel to
Goens, Jean   +11 more
core   +1 more source

An approach to acanthosis nigricans

open access: yesIndian Dermatology Online Journal, 2014
Acanthosis nigricans (AN) is characterized by dark, coarse and thickened skin with a velvety texture, being symmetrically distributed on the neck, the axillae, antecubital and popliteal fossae, and groin folds, histopathologically characterized by ...
Meghana Madhukar Phiske
doaj   +1 more source

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

open access: yesInternational Journal of Dermatology, Volume 65, Issue 3, Page 464-488, March 2026.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla   +8 more
wiley   +1 more source

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