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      Cutaneous calciphylaxis: a retrospective histopathologic evaluation.

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          Abstract

          Calciphylaxis is a rare and life-threatening disease characterized by cutaneous necrosis and vascular calcification. Often, skin biopsy specimens are not diagnostic because of the limited depth of the specimen, biopsy site, and clinical stage. To better understand the utility of various histologic features in rendering the diagnosis of calciphylaxis and to compare von Kossa versus Alizarin red stains in the detection of calcium deposits, we retrospectively analyzed the histologic features and histochemical stain findings of 56 skin biopsies from 27 consecutive patients seen at Massachusetts General Hospital from October 2002 to April 2012, with confirmed diagnosis of calciphylaxis and compared with that of 19 skin biopsies from 17 patients with other disease processes. All forms of vascular calcification and vascular thrombosis were significantly associated with cutaneous calciphylaxis. Perieccrine calcium deposition, highly specific to calciphylaxis, was the only form of calcium deposition noted in 4 (7%) skin biopsies from patients with calciphylaxis. Although the staining appears to be comparable, the deposits seen on Alizarin red appeared larger and were birefringent. Although subtle, perieccrine calcification may aid in the diagnosis of calciphylaxis in settings where typical vascular and extravascular calcification are not identified. Performing both von Kossa and Alizarin red stains might increase the detection of calcium deposit.

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          Author and article information

          Journal
          Am J Dermatopathol
          The American Journal of dermatopathology
          1533-0311
          0193-1091
          Jul 2013
          : 35
          : 5
          Affiliations
          [1 ] Department of Pathology, Harvard Medical School and Massachusetts General Hospital, Boston, MA 02114, USA.
          Article
          10.1097/DAD.0b013e31827c7f5d
          23328789
          045841b3-a52b-4579-b944-80938edb8155
          History

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