Two cases in a family with the diagnosis of pachydermoperiostosis mimicking acromegaly

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Two cases in a family with the diagnosis of pachydermoperiostosis mimicking acromegaly

Abstract is not required for Clinical Imagesis not required for Clinical Images (This page in not part of the published article.) International Journal of Case Reports and Images, Vol. 5 No. 10, October 2014. ISSN – [0976-3198] Int J Case Rep Images 2014;5(10):727–730. www.ijcasereportsandimages.com Kutbay et al. 727 CLINICAL IMAGES OPEN ACCESS Two cases in a family with the diagnosis of pachyd...

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Primary Pachydermoperiostosis and report of two cases in a family

Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by folded coarse skin, hyperostosis, clubbing of fingers and abnormalities in other organs such as gastrointestinal tract. Because of safety parents guides us to familial incidence and penetration of gene in 50% of cases. Diagnosis is based on clinical and radiological findings. Males are more susceptible than females to thi...

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Pachydermoperiostosis: Incomplete form, mimicking acromegaly

Sir, Read with interest the article, prevalence of colonic polyp and its predictors in patients with acromegaly. [1] Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare disorder that is characterized by digital clubbing and subperiosteal new bone formation associated with pain, polyarthiritis, cutis verticis gyrata, seborrhea, and hyperhidrosis. It is important to the...

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Pachydermoperiostosis Masquerading as Acromegaly

Context Acromegaly usually is suspected on clinical grounds. Biochemical confirmation is required to optimize therapy, but there are other differential diagnoses. Case Description We describe a 24-year-old Uzbek man who presented with many clinical symptoms and signs of apparent acromegaly. On examination, the patient showed a rugose folding of his scalp, with the formation of tender, painful...

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ژورنال

عنوان ژورنال: International Journal of Case Reports and Images

سال: 2014

ISSN: 0976-3198

DOI: 10.5348/ijcri-201463-cl-10051