Pachydermoperiostosis Mimicking Acromegaly: A Case Report

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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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Pachydermoperiostosis in a patient with chronic hepatitis B virus infection referred as acromegaly: a case report

BACKGROUND Primary hypertrophic osteoarthropathy also known as pachydermoperiostosis is a rare genetic disorder that has often been confused with acromegaly because of similar clinical features. Vascular endothelial growth factors which have been implicated in the clinical features of pachydermoperiostosis, have also been shown to be present in chronic hepatitis and implicated in the malignant ...

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Pachydermoperiostosis: a rare mimicker of acromegaly

Pachydermoperiostosis is a very rare osteoarthrodermopathic disorder whose clinical and radiographic presentations may mimic those of acromegaly. In the evaluation of patients with acromegaloid appearances, pachydermoperiostosis should be considered as a differential diagnosis. In this article, we report a 17-year-old boy who presented with 2-year history of acral enlargement and facial appeara...

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ژورنال

عنوان ژورنال: Turkish Journal of Rheumatology

سال: 2012

ISSN: 1309-0291,1309-0283

DOI: 10.5606/tjr.2012.020