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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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 complicated with myelofibrosis and compound heterozygous SLCO2A1 mutations: a case report and review of literature [PDF]
Frontiers in OncologyBackgroundPrimary hypertrophic osteoarthropathy (PHO) is a rare hereditary clinical syndrome characterized by digital clubbing, periostosis, and pachydermia.
Qirui Xu +4 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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Anales de la Facultad de MedicinaPachydermoperiostosis, also known as primary hypertrophic osteoarthropathy, is a rare hereditary disease characterized by soft tissue proliferation and periosteal new bone formation in long bones, classically presenting with digital clubbing, symmetric
Victor Sudário Takahashi +3 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 Cunha
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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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Cutis Verticis Gyrata Across the Diagnostic Spectrum: Two Cases Highlighting Challenges in Clinical Classification [PDF]
Clinical Case ReportsCutis verticis gyrata (CVG) is an uncommon disorder characterized by cerebriform thickening of the scalp that may occur as a primary condition or secondary to a variety of systemic disorders.
Sanket Bishokarma +2 more
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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
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