Ariza A, López M D, Mate J L, Curós A, Villagrasa M, Navas-Palacios J J
Department of Anatomic Pathology, Hospital Universitari Germans Trias i Pujol, Barcelona, Spain.
Hum Pathol. 1995 Jan;26(1):121-3. doi: 10.1016/0046-8177(95)90124-8.
Giant cell myocarditis (GCM) is a rare condition whose histologic hallmark, the multinucleate giant cell, is of debated origin (monocytic v myogenic). We report the case of a 46-year-old woman with a previous diagnosis of ulcerative colitis who rapidly deteriorated and died as the result of refractory ventricular tachyarrhythmias. Postmortem examination showed a diffuse infiltration of the myocardium by round cells and multinucleate giant cells. Immunohistochemically, round cells were demonstrated to be T lymphocytes admixed with monocytes. Multinucleate giant cells expressed monocytic markers (MAC 387, lysozyme) and were negative for muscle markers (actin, desmin, myoglobin). This case illustrates the monocytic and macrophagic nature of multinucleate giant cells and lends support to the autoimmune hypothesis of GCM by the concurrence of the latter with ulcerative colitis.
巨细胞性心肌炎(GCM)是一种罕见疾病,其组织学特征性表现为多核巨细胞,但其起源(单核细胞源性与肌源性)存在争议。我们报告一例46岁女性病例,该患者既往诊断为溃疡性结肠炎,因难治性室性快速心律失常迅速病情恶化并死亡。尸检显示心肌有圆形细胞和多核巨细胞弥漫性浸润。免疫组化显示,圆形细胞为T淋巴细胞,混有单核细胞。多核巨细胞表达单核细胞标志物(MAC 387、溶菌酶),而肌肉标志物(肌动蛋白、结蛋白、肌红蛋白)呈阴性。该病例说明了多核巨细胞的单核细胞和巨噬细胞性质,并因GCM与溃疡性结肠炎并存而支持了GCM的自身免疫假说。