Background: There is scant literature that documents pseudoxanthoma elasticum (PXE)-like histologic changes in the setting of inflammatory skin diseases. This article documents granulomatous dermatitis with PXE-like changes in a patient with cystic fibrosis. This is the first report of its kind, to our knowledge.

Observations: A 33-year-old woman with cystic fibrosis developed a papular eruption on the flexural surfaces of the upper and lower extremities, which was initially treated with prednisone. A punch biopsy showed granulomatous inflammation and associated PXE-like changes. The combined histologic and clinical findings were most consistent with granuloma annulare. There was no family history of PXE or clinical manifestations of PXE. The rash gradually resolved itself over the next several months.

Conclusions: There are few publications that document PXE-like changes in association with various inflammatory skin conditions. Thus, the clinical significance of this finding remains uncertain. This case and previous reports are discussed in the context of current molecular and genetic knowledge. It is hoped that greater awareness of this phenomenon will promote further investigation and elucidation of the clinical and biologic significance of PXE-like changes observed in biopsies of inflammatory skin disorders.

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http://dx.doi.org/10.1001/archdermatol.2009.238DOI Listing

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Article Synopsis
  • - Pseudoxanthoma elasticum (PXE) is a genetic disorder affecting skin, eyes, and blood vessels, mainly caused by mutations in the ABCC6 gene that lead to impaired calcium regulation in the body.
  • - The study examined five patients from unrelated families with biallelic variants in the GGCX gene, associated with PXE-like symptoms, using next-generation sequencing for diagnosis.
  • - Findings indicate that GGCX variants can also cause PXE characteristics and that patients' plasma levels of inorganic pyrophosphate (PPi) remain normal, challenging the idea that PPi levels are responsible for ectopic calcification in GGCX deficiency.
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Article Synopsis
  • * The condition usually appears during the teenage years and is primarily caused by mutations in specific genes, with most cases being sporadic or recessive.
  • * Recent research has identified several disorders that display PXE-like symptoms or microscopic features, prompting a discussion on the potential mechanisms that could cause this overlap.
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Pseudoxanthoma elasticum (PXE) is an autosomal recessive genetic disorder characterized by aberrant fragmentation and calcification of elastic fibers, leading to characteristic cutaneous, ophthalmic, and cardiovascular manifestations. PXE demonstrates significant phenotypic variability; involvement of the oral mucosa may be the only clue to the diagnosis. Reports on mucous membrane involvement in PXE are scarce.

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Background: Attempts have been made to establish discriminative criteria between classic calciphylaxis (CPX) and those cases in which cutaneous vascular calcification (CVC) represents an incidental finding (epiphenomenon).

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Calciphylaxis, otherwise known as calcific uremic arteriolopathy, is an aggressive disease characterized by painful, ischemic skin lesions with histologic findings of microvascular calcification involving the fat. It is most commonly seen in patients with end-stage renal disease who are on dialysis. Early diagnosis is pivotal for optimal management.

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