Inflammatory bowel disease‐related periostosis
Rheumatology & Autoimmunity, 2022 Key point Periosteal reaction and bone absorption could be manifested in ulcerative colitis.
Yilin Yuan, Rong Mu
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Hypertrophic Osteoarthropathy Associated with Probable Smear-Negative Pulmonary Tuberculosis [PDF]
Case Reports in Rheumatology, 2022 Association of hypertrophic osteoarthropathy (HOA) with pulmonary tuberculosis is rarely reported, especially with smear-negative pulmonary tuberculosis (SNPT), in which its diagnosis is a challenge.
Mohamed Ahmed Ghassem +5 more
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Frontal lifting using a tissue expander in pachydermoperiostosis: A case report
Clinical Case Reports (discontinued), 2021 Pachydermoperiostosis, a rare condition, is characterized by pachydermia, finger clubbing, and periostosis. We present an unusual treatment for frontal rhytids, for which we used a tissue expander that contributed to thinning of the skin and the depth of
Daniel José Dias Cunha
exaly +3 more sources
Clinical and Genetic Characteristics of Korean Patients Diagnosed with Chronic Enteropathy Associated with SLCO2A1 Gene: A KASID Multicenter Study [PDF]
Gut and Liver, 2022 Background/Aims: Chronic enteropathy associated with SLCO2A1 gene (CEAS), an inherited disease characterized by nonspecific intestinal ulcers, has emerged in the Japanese population via loss-of-function mutations in the SLCO2A1 gene.
Hee Seung Hong +17 more
doaj +5 more sources
Pachydermoperiostosis Mimicking Inflammatory Arthritis: Case Description and Narrative Review [PDF]
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 +7 more
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A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly [PDF]
Bone Reports, 2023 Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. We describe a Japanese male patient with PDP who was differentially diagnosed with acromegaly by identification of compound ...
Yukako Nakano +5 more
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Primary hypertrophic osteoarthropathy: genetics, clinical features and management [PDF]
Frontiers in Endocrinology, 2023 Primary hypertrophic osteoarthropathy (PHO) is a genetic disorder mainly characterized by clubbing fingers, pachydermia and periostosis. Mutations in the HPGD or SLCO2A1 gene lead to impaired prostaglandin E2 (PGE2) degradation, thus elevating PGE2 ...
Qi Lu +4 more
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Un enterramiento colectivo en cueva del III milenio AC en el centro de la Península Ibérica: el Rebollosillo (Torrelaguna, Madrid) [PDF]
Trabajos de Prehistoria, 2017 El Rebollosillo es una pequeña cueva kárstica situada en el centro de la Península Ibérica utilizada para la disposición de enterramientos secundarios en la mitad del III milenio AC. Presentamos resultados bioantropológicos, isotópicos (87Sr/86Sr, δ13C y
Pedro Díaz-del-Río +12 more
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A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma [PDF]
Clinical, Cosmetic and Investigational Dermatology, 2023 Yan Jing Chen, Li Li Department of Dermatology and Venereology, West China Hospital, Sichuan University, Chengdu, Sichuan, People’s Republic of ChinaCorrespondence: Li Li, Department of dermatology and venereology, West China Hospital, Sichuan University,
Chen YJ, Li L
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Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review [PDF]
Case Reports in DermatologyIntroduction: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of pachydermia (thickening of skin) and periostosis (new bone formation).
Haibo Zhao +3 more
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