Results 51 to 60 of about 635 (170)

Earliest Detection of Oral Cancer Using Non‐Invasive Brush Biopsy Including DNA‐Image‐Cytometry: Report on Four Cases

Analytical Cellular Pathology, Volume 25, Issue 4, Page 159-166, 2003., 2003
Objective: We describe four patients presenting early oral cancers, detected cytologically on non‐invasive brush biopsies including DNA‐image cytometry as an adjunctive method before histology on scalpel biopsies confirmed the evidence of malignancy. Methods: Brush biopsies were performed and smears thereof investigated cytologically.
Torsten W. Remmerbach, Horst Weidenbach, Alexander Hemprich, Alfred Böcking   +3 more
wiley   +1 more source

Cutis Verticis Gyrata Differential Diagnosis: Clinical Case

Вопросы современной педиатрии
Background. Cutis verticis gyrata is rare benign scalp disorder characterized by excessive skin and subcutaneous tissue proliferation and hypertrophy. Nowadays, there are three forms of this disease with various developmental mechanisms and associated ...
Tatiana S. Belysheva, Ekaterina E. Zelenova, Tatiana A. Gassan, Eduard T. Ambarchyan, Malika I. Denieva, Yana V. Vishnevskaya, Tatiana V. Nasedkina, Nikolay N. Murashkin   +7 more
doaj   +1 more source

Touraine Solente Gole syndrome: The elephant skin disease

Indian Journal of Plastic Surgery, 2013
Touraine Solente Gole syndrome is a rare hereditary syndrome of primary pachydermoperiostosis, with the characteristic triad of pachydermia (or elephant like skin), periostosis and acropachia.
T. M. Sheeja Rajan, N. C. Sreekumar, S. Sarita, K. R. Thushara   +3 more
doaj   +1 more source

Pachydermoperiostosis (Touraine-Solente-Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy

Journal of the Dow University of Health Sciences
Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is an autosomal dominant genetic disorder that is rare and is identified by finger clubbing, skin thickening, and periosteal ...
Fatima Khurshid, Kinza Shahid Randhawa, Fatima Khurshid, Memoona Khalid   +3 more
doaj   +9 more sources

The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation

Endocrine Connections, 2019
Background: Primary hypertrophic osteoarthropathy (PHO) is a rare genetic multi-organic disease characterized by digital clubbing, periostosis and pachydermia. Two genes, HPGD and SLCO2A1, which encodes 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and
Qianqian Pang, Yuping Xu, Xuan Qi, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Ling Qin, Weibo Xia   +8 more
doaj   +1 more source

Pachydermoperiostosis Mimicking Inflammatory Arthritis: Case Description and Narrative Review

Rheumato, 2023
Pachydermoperiostosis (PDP), also called primary hypertrophic osteoarthropathy (HOA), is a rare genetic disease with typical thickening of the skin (pachydermia) and rheumatic manifestations, with clubbing of the fingers and toes and periostosis of the ...
AKM Kamruzzaman, Maisha Farzana, Md Mainuddin Sohel, Emrul Kaiser, Nobendu Chowdhury, Md Hafizur Rahman, Syed Atiqul Haq, Johannes J. Rasker   +7 more
doaj   +1 more source

Where Do Core Thalamocortical Axons Terminate in Mammalian Neocortex When There Is No Cytoarchitecturally Distinct Layer 4?

Journal of Comparative Neurology, Volume 532, Issue 7, July 2024.
Immunohistochemical staining for vesicular glutamate transporter 2 reveals the “core” thalamocortical projection to the neocortex in the African elephant. In the elephant and other mammals with unusual skin (such as pachydermatous skin), layer 4 is cytoarchitecturally indistinct, possibly absent, and the thalamocortical input terminates primarily on ...
Adhil Bhagwandin, Zoltán Molnár, Mads F. Bertelsen, Karl Æ. Karlsson, Abdulaziz N. Alagaili, Nigel C. Bennett, Patrick R. Hof, Consolate Kaswera‐Kyamakya, Emmanuel Gilissen, Jaikishan Jayakumar, Paul R. Manger   +10 more
wiley   +1 more source

Paquidermoperiostose: forma completa da síndrome Pachydermoperiostosis: the complete form of the syndrome

Anais Brasileiros de Dermatologia, 2011
A paquidermoperiostose é uma genodermatose rara, com apresentações clínicas variadas, que se apresenta com espessamento cutâneo, baqueteamento digital e periostose. Apresenta patogênese ainda incerta e acomete, principalmente, homens. Descreve-se caso de
Marina Besen Guerini, Mariana Tremel Barbato, Naiana Bittencourt de Sá, Daniel Holthausen Nunes, Paulo Roberto Zeni   +4 more
doaj   +1 more source

Pseudoacromegaly—A challenging entity in the endocrine clinic: A systematic review

Clinical Endocrinology, Volume 100, Issue 6, Page 542-557, June 2024.
Abstract Objective Pseudoacromegaly encompasses conditions with features of acromegaly/gigantism, but no growth hormone (GH) or insulin‐like growth factor‐1 (IGF‐1) excess. We aimed to review published pseudoacromegaly cases evaluated due to clinical suspicion of acromegaly.
Pedro Marques, Inês Sapinho, Márta Korbonits   +2 more
wiley   +1 more source

Hypertrophy of the feet and ankles presenting in primary hypertrophic osteoarthropathy or pachydermoperiostosis: a case report

Journal of Medical Case Reports, 2012
Introduction Pachydermoperiostosis or primary hypertrophic osteoathropathy is a rare genetic disease with autosomal transmission. This disorder, which affects both bones and skin, is characterized by the association of dermatologic changes (pachydermia ...
Akrout Rim, Bendjemaa Samar, Fourati Héla, Ezzeddine Mariem, Hachicha Imene, Baklouti Soufiene   +5 more
doaj   +1 more source