scholarly journals Pedunculated Pulmonary Parenchymal Leiomyoma Associated with Hypertrophic Osteoarthropathy: Case Report

2014 ◽  
Vol 7 (1) ◽  
pp. 6-10
Author(s):  
Leonardo Politi ◽  
Camilla E. Comin ◽  
Daniel Barale ◽  
Andrea Lopez Pegna
Keyword(s):  
Case Report ◽  
Hypertrophic Osteoarthropathy

scholarly journals Pachydermoperiostosis (PDP): A Case Report

2021 ◽  
pp. 1-8
Author(s):  
Abdulameer M. Abu Nailah ◽  
Islam A. M. Abu-Nayla ◽  
Umniyah A. M. Abu-Nayla
Keyword(s):  
Case Report ◽  
Hypertrophic Osteoarthropathy ◽  
Primary Hypertrophic Osteoarthropathy ◽  
Digital Clubbing ◽  
Cutis Verticis Gyrata ◽  
Incomplete Form ◽  
Bone Abnormalities ◽  
Primary Form

Abstract Pachydermoperiostosis (PDP) is the primary form of hypertrophic osteoarthropathy which accounts for 5% of all cases of the disorder. It is a rare hereditary disorder that is associated with digital clubbing, polyarthritis, cutis verticis gyrata, Seborrhea, eyelid ptosis, and hyperhidrosis. In this case report, we discussed a case of an incomplete form of primary hypertrophic osteoarthropathy characterised by evidence of bone abnormalities without pachydermia. Keywords: Pachydermoperiostosis, hypertrophic osteoarthropathy, periostosis.

scholarly journals Primary idiopathic hypertrophic osteoarthropathy in a child: characteristics of the disease with a case report

2017 ◽  
Vol 11 (4) ◽  
pp. 40-47
Author(s):  
N. A. Lyubimova ◽  
L. S. Snegireva ◽  
N. A. Terentyev ◽  
R. V. Idrisova ◽  
V. V. Avramenko ◽  
...  
Keyword(s):  
Case Report ◽  
Hypertrophic Osteoarthropathy ◽  
Child Characteristics

scholarly journals Case report: Schizophrenia and hypertrophic osteoarthropathy, a rare syndrome hiding a life-threatening condition

2021 ◽  
Author(s):  
emna Baklouti ◽  
Mehdi Karoui ◽  
rania kammoun ◽  
Faten Ellouze
Keyword(s):  
Lung Cancer ◽  
Case Report ◽  
Paraneoplastic Syndrome ◽  
Hypertrophic Osteoarthropathy ◽  
Rare Syndrome ◽  
Threatening Condition ◽  
Life Threatening ◽  
Somatic Disorders ◽  
Cardio Vascular

Schizophrenia is associated to somatic disorders especially cardio-vascular and auto-immune. Through this case report, we describe an association with hypertrophic osteoarthropathy (HPO). For this patient it was a paraneoplastic paraneoplastic syndrome secondary to lung cancer. This syndrome is rare but important to recognize since it could hide a life-threatening condition.

scholarly journals Hypertrophic osteoarthropathy (HOA) in a child with congenital cyanotic heart disease - a case report

2016 ◽  
Vol 1 (5) ◽  
Author(s):  
Michelo S Choopa ◽  
Belinda Mitchell ◽  
Ignatius T Menyatsoe ◽  
Gertruida van Biljon
Keyword(s):  
Heart Disease ◽  
Case Report ◽  
Hypertrophic Osteoarthropathy ◽  
Cyanotic Heart Disease ◽  
Congenital Cyanotic Heart Disease

scholarly journals A male Korean who was diagnosed with chronic enteropathy associated with SLCO2A1 (CEAS): case report with literature review

2018 ◽  
Vol 5 (1) ◽  
pp. e000223 ◽  
Author(s):  
Xi Sun ◽  
Naoki Hosoe ◽  
Ryoichi Miyanaga ◽  
Kayoko Kimura ◽  
Shinta Mizuno ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Point Mutations ◽  
Gene Mutations ◽  
Occult Blood ◽  
Faecal Occult Blood Test ◽  
Tertiary Hospital ◽  
Hypertrophic Osteoarthropathy ◽  
Chronic Enteropathy ◽  
Two Sides

ObjectiveTo further disseminate the nomenclature of chronic enteropathy associated with SLCO2A1 (CEAS), especially for physicians in China and Korea where the genetic feature of SLCO2A1 gene mutations related hypertrophic osteoarthropathy and pachydermia had been extensively studied. SLCO2A1 gene mutations related hypertrophic osteoarthropathy and pachydermia had been extensively studied.DesignA case report with literature review of SLCO2A1 gene mutations-related disorders.ResultsA 38-year-old Korean presented to a tertiary hospital with dizziness, abdominal pain and melena. He had a positive faecal occult blood test on initial workup. Oesophagogastroduodenal endoscopy (OGD), colonoscopy and CT scan were unremarkable and showed no obvious cause for his melena. Capsule endoscope and roentgen barium studies were performed, revealing an erythematous mucosa with ulcers in the jejunum and stenosis to the jejunal–ileal junction. Next-generation sequencing was then performed and discovered point mutations of SLCO2A1 gene’s seven exon (940+1 G>A) and 13 exon (1807 C>T) allele. This Korean patient with CEAS is the first documented case noted outside of the Japanese population.ConclusionCEAS is not uniquely found in Japanese individuals. There are lots of similarities between CEAS and primary hypertrophic osteoarthropathy, the two entity may just be the two sides of one same coin. International and multidisciplined efforts are required to further study this complicated disorder.

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