Nuno-Gonzalez Almudena, Calzado-Villarreal Leticia, Gutierrez-Pascual Marta, Gamo-Villegas Reyes, Sanz-Robles Henar, Sanchez-Gilo Araceli, Pinedo-Moraleda Fernando, Lopez-Estebaranz Jose Luis
Hospital Universitario Fundacion Alcorcon, Alcorcon, Madrid, Spain.
Dermatol Online J. 2011 Nov 15;17(11):4.
In 1988, Tumiati et al described the first case of calcinosis cutis related to a calcium-containing heparin. Since then, only 18 cases have been reported in the literature; they usually have an altered calcium-phosphate product, an elevated parathyroid hormone (PTH), or both. We report a 33-year-old patient who developed calcinosis cutis at sites of nadroparin injections without any disturbance of calcium-phosphate product, PTH, or vitamin D. The pathogenesis of calcinosis cutis secondary to nadroparin injections remains controversial; Proposed causes included metastatic, dystrophic, iatrogenic, or multifactorial etiologies. This is the first case of multiple nodules of calcinosis cutis without alterations of calcium-phosphate product, PTH, or vitamin D, which supports an iatrogenic mechanism. We also suggest that calcinosis cutis could be more frequent than we thought and is probably an underdiagnosed entity.
1988年,图米亚蒂等人描述了首例与含钙肝素相关的皮肤钙化病例。从那时起,文献中仅报道了18例;这些病例通常存在钙磷乘积改变、甲状旁腺激素(PTH)升高,或两者皆有。我们报告了一名33岁的患者,其在那屈肝素注射部位出现了皮肤钙化,而钙磷乘积、PTH或维生素D均无任何异常。那屈肝素注射继发皮肤钙化的发病机制仍存在争议;提出的病因包括转移性、营养不良性、医源性或多因素病因。这是首例钙磷乘积、PTH或维生素D无改变的多发性皮肤钙化结节病例,支持医源性机制。我们还认为,皮肤钙化可能比我们想象的更常见,可能是一种诊断不足的疾病。