Pachydermoperiostosis associated with gastric neoplasia
Revista da Associação Médica Brasileira, 2011 , among others.More than 20% of the patients with PDP have hyper-trophic gastritis or gastric ulcer and some of them have high pepsinogen levels. Other diseases of the gastric sys-tem can be considered occasional associations, such as gastric polyposis, Crohn’s disease and protein-losing en ...
Rafael Valentini +5 more
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Journal Of World SciencePachydermoperiostosis is a genetic disorder characterized by pachydermia and periostosis. The clinical and radiological features of pachydermoperiostosis are similar to acromegaly. The Prevalence of pachydermoperiostosis is estimated 0.16%.
Saiful Anam, Hemi Sinorita
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Cutis verticis gyrata in a patient with multiple basal cell carcinomas; case presentation and review of the literature [PDF]
, 2016 Cutis verticis gyrata is a rare disease characterized by convoluted folds and deep furrows of the scalp, resembling the gyri and sulci of the cerebral cortex.
Benea, Vasile +6 more
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Pachydermoperiostosis-critical analysis with report of five unusual cases [PDF]
, 2020 Pachydermoperiostosis (idiopathic hypertrophic arthropathy) {MIM 167100} is an uncommon disease characterized by unique phenotype (digital clubbing and pachydermia) and distinctive radiographic appearances (periostosis).
Anna Latos-Bielenska +5 more
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Vitiligo at Injection Site of PEG-IFN-α 2a in Two Patients with Chronic Hepatitis C: Case Report and Literature Review [PDF]
, 2010 A 72-year-old female and a 57-year-old male with chronic hepatitis C were treated with a combination therapy of pegylated interferon (PEG-IFN)-α 2a (180 μg s.c. once a week) and ribavirin (1,000 mg orally daily).
Arya, S. +4 more
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HYPERTROPHIC OSTEOARTHROPATHY IN A PATIENT WITH HETEROZYGOUS MUTATION IN THE SLCO2A1 GENE: A CASE REPORT [PDF]
, 2023 Hypertrophic osteoarthropathy (HOA) is a condition characterized by aberrant skin and osseous tissue proliferation in the distal extremities. Mutations in the 15-hydroxyprostaglandin dehydrogenase gene (HPGD) and the soluble carrier organic anion carrier
Ilke Coskun Benlidayi +2 more
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A Rare Case: Touraine Solente Gole Syndrome
Haseki Tıp Bülteni, 2017 Touraine-Solente-Gole syndrome, also known as pachydermoperiostosis, is transmitted as an autosomal recessive trait. It is characterized by enlargement of fingers and toes, pachyderma, excessive sweating, and pain.
Kamil Şahin +4 more
doaj +1 more source
Диференційна діагностика гіпертрофічної остеоартропатії (огляд літератури та власне спостереження) [PDF]
, 2010 У статті узагальнено дані літератури щодо диференційної діа- гностики вторинної та первинної гіпертрофічної остеартропатії. Продемонстровано клінічний випадок запізнілої діагностики рідкісного варіанта гіпертрофічної остеоартропатії ...
Bushman, Svitlana Vasylivna +29 more
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One-sided brain over the head: Cutis verticis gyrata
Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2018 Cutis verticis gyrata (CVG) is a rare disease manifesting as convoluted folds and furrows, resembling sulci and gyri formed from thickened skin of the scalp. It can be congenital or acquired and primary or secondary.
Priyanka Date, Sonia Jain
doaj +1 more source
Pachydermoperiostosis successfully treated with celecoxib
Journal of dermatology (Print)Hiroki Yamamoto +5 more
openalex +2 more sources