Results 61 to 70 of about 2,571 (160)

Laugier–Hunziker syndrome: A case report

Pigment International
Laugier–Hunziker syndrome (LHS) is a rare, benign pigmentary disorder characterized by unique pigmentation over mucosa, nails, and acral sites, arising spontaneously during adulthood. It has no malignant potential or systemic involvement. It has a female
Zigu S. Krishn, Yogesh Devaraj, Mukunda Ranga Swaroop, Rashmi Rameshchandra Mallya, Neethu Nag, Kadari Yashwanth Reddy   +5 more
doaj   +1 more source

Colorectal Precancerous Lesions: Molecular Mechanisms, Research Tools, and Natural Product‐Based Clinical Translation

MedComm – Oncology, Volume 5, Issue 2, June 2026.
This article systematically elucidates the molecular mechanisms of colorectal precancerous lesions, introduces cutting‐edge research tools like multi‐omics and organoids, and highlights the potential and prospects of natural products such as berberine, resveratrol, and curcumin in preventing and intervening in colorectal carcinogenesis by modulating ...
Shunji Liu, Chujuan Cui, Lingdong Kong, Qiang Xu, Haibo Cheng, Lisha Zhou, Yang Sun   +6 more
wiley   +1 more source

Dyskeratosis Congenita Associated Non-Specific Interstitial Pneumonia [PDF]

Journal of Krishna Institute of Medical Sciences University, 2017
Dyskeratosis Congenita (DC) is a rare inherited disorder of ectodermal dysplasia. It consists of a classical mucocutaneous triad of abnormal skin pigmentation, nail dystrophy and leukoplakia. Pulmonary disease is seen in 10-15%.
Unnati D. Desai , Jyotsna M. Joshi
doaj  

Melaena with Peutz-Jeghers syndrome: a case report

Journal of Medical Case Reports, 2010
Introduction Peutz-Jeghers syndrome (PJS) is a rare familial disorder characterised by mucocutaneous pigmentation, gastrointestinal and extragastrointestinal hamartomatous polyps and an increased risk of malignancy.
Morrissey John R, Palit Amitabh, Nangalia Ramlal, Mahapatra Sunondo R, Bhattacharya Sayantan, Ruban Ernie, Jadhav Vijay, Mathew George   +7 more
doaj   +1 more source

Peutz-Jeghers syndrome: A circumventable emergency

Indian Journal of Dermatology, 2018
Peutz-Jeghers syndrome (PJS) is characterized by multiple hamartomatous polyps in the gastrointestinal tract and mucocutaneous pigmentation. Here we present, a case of multiple gastrointestinal hamartomatous polyps in a 22-year-old male who had been ...
Sourav Choudhury, Anupam Das, Priyankar Misra, Udipta Ray, Sujata Sarangi   +4 more
doaj   +1 more source

Cancer problem in Peutz-Jeghers syndrome

Advanced Biomedical Research, 2013
Peutz-Jeghers syndrome is a rare autosomal dominantly inherited condition, characterized by the presence of hamartomatous gastrointestinal polyps and mucocutaneous pigmentation.
Diana Taheri, Noushin Afshar-Moghadam, Parvin Mahzoni, Amin Eftekhari, Seyed Mozafar Hashemi, Mohammad Hasan Emami, Mehdi Fesharakizadeh, Hamid Reza Ghasemi-basir   +7 more
doaj   +1 more source

A young woman with mucocutaneous pigmentation and intestinal polyps [PDF]

Hong Kong Medical Journal, 2013
H M, Luk, Ivan F M, Lo, Kelvin M C, Yu, Tony M F, Tong, Stephen T S, Lam   +4 more
openaire   +2 more sources

Peutz-Jeghers Syndrome: In Siblings with Palmer-Plantar Pigmentation

Journal of Indian Academy of Oral Medicine and Radiology, 2011
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmented perioral maculesn pigmented spots in the oral mucosa and digits along with hamartomatous polyps in the gastrointestinal tract.
K V Suresh, Prashanth Shenai, Laxmikanth Chatra   +2 more
doaj   +1 more source

Sindrome de Peutz-Jeghers. Diversidade de expressão gastrointestinal em idade pediátrica e considerações sobre a sua abordagem clínica.

Acta Médica Portuguesa, 2004
Peutz-Jeghers syndrome is a rare autosomal dominant condition, characterized by gastrointestinal polyposis, mucocutaneous pigmentation and high risk of neoplasia in multiple organs.
Ana I Lopes, Juan Gonçalves, Ana M Palha, Fátima Furtado, António Marques   +4 more
doaj   +1 more source

Q-Switched Laser for the treatment of mucocutaneous pigmentation on Peutz-Jeghers Syndrome

Surgical & Cosmetic Dermatology, 2022
Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant disease where there is a mutation in the tumor suppressor gene, with a greater predisposition to neoplasms, especially of the gastrointestinal tract. The first manifestations begin during childhood with the presence of mucocutaneous melanosis and, later, gastrointestinal hamartomatous polyps ...
Abdo Salomão, Constança Pithon Pereira, Rodrigo Cesar Davanco, Daniella Grande Curi, Domingos Jordão   +4 more
openaire   +1 more source