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Clinicopathologic Features and Calcium Deposition Patterns in Calciphylaxis: Comparison With Gangrene, Peripheral
Emily R McMullen1, Paul W Harms1,2, Lori Lowe1,2
1Departments of Pathology.
Insights
Diagnosing calciphylaxis requires identifying vascular calcification and thrombosis. Combining von Kossa stain findings with small vessel thrombosis offers high sensitivity and specificity for calciphylaxis diagnosis.
Area of Science:
- Pathology
- Vascular Biology
- Dermatology
Background:
- Calciphylaxis diagnosis is challenging due to overlapping features with other vascular diseases.
- Vascular calcification and thrombosis are key, but their patterns in other conditions are unclear.
- The diagnostic specificity of fine calcium deposits and extravascular calcifications needs clarification.
Purpose of the Study:
- To identify clinicopathologic discriminators for calciphylaxis.
- To compare features across calciphylaxis, gangrene, chronic stasis, and thrombotic vasculopathy.
- To evaluate the utility of specific staining and histopathological findings.
Main Methods:
- Retrospective analysis of clinicopathologic features in 4 patient groups.
- Inclusion of calciphylaxis (n=27), gangrene (n=20), viable skin (n=20), chronic stasis (n=22), and thrombotic vasculopathy (n=19).
- Histopathological examination including hematoxylin and eosin and von Kossa (VK) staining.
Main Results:
- Subcutaneous small vessel calcification on H&E had low sensitivity (56%) but relative specificity for calciphylaxis.
- VK staining detected fine calcium deposits, but specificity was limited by peripheral artery disease.
- Combining VK-detected calcification with subcutaneous small vessel thrombosis yielded optimal sensitivity (85%) and specificity (88%).
- Diffuse dermal angiomatosis was exclusively observed in calciphylaxis.
- Calcification of eccrine glands, elastic fibers, and perineurium were not specific discriminators.
Conclusions:
- Von Kossa (VK) stain aids in detecting vascular calcification, preventing false negatives.
- A diagnosis of calciphylaxis requires concomitant subcutaneous small vessel thrombosis alongside VK findings.
- Diffuse dermal angiomatosis suggests calciphylaxis and warrants deeper tissue sampling.
Abstract:
Diagnosis of calciphylaxis is crucial, yet its distinction from other vascular diseases can be challenging. Although vascular calcification and thrombosis are hallmarks of calciphylaxis, the incidence and patterns of these features in other vascular diseases have not been well characterized. The specificity of fine calcium deposits in vessel walls (identifiable on von Kossa [VK] stain only) and other extravascular calcifications is not entirely clear. We retrospectively examined the clinicopathologic features in calciphylaxis (n=27), gangrene and viable skin at amputation margin (n=20 each), chronic stasis (n=22), and thrombotic vasculopathy (n=19) to identify useful discriminators. Calcification of subcutaneous small vessels appreciable on hematoxylin and eosin stain was relatively specific for calciphylaxis, although sensitivity was low (56%). VK detected fine calcium deposits in vessel walls not appreciable on hematoxylin and eosin, however, specificity was limited by frequent finding of similar deposits in peripheral artery disease. Combining calcium deposits detected by VK and thrombosis of subcutaneous small vessels resulted in optimal sensitivity (85%) and specificity (88%) for calciphylaxis. Similar observations applied to medium-sized vessel calcification. Calcification of eccrine gland basement membranes, elastic fibers, and perineurium did not effectively distinguish calciphylaxis from other groups. Diffuse dermal angiomatosis was exclusively found in calciphylaxis in this study. In conclusion, VK is useful in enhancing the detection of vascular calcification and avoiding the false-negative diagnosis, but this finding requires concomitant subcutaneous small vessel thrombosis to support a diagnosis of calciphylaxis. Diffuse dermal angiomatosis should increase suspicion for underlying calciphylaxis and prompt deeper sampling in the appropriate clinical setting.
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