Aroukatos Panagiotis, Verras Dionysios, Vandoros Gerassimos P, Repanti Maria
Department of Pathology, "Agios Andreas" General Hospital, Tsertidou 1, 26 335 Patras, Greece.
Case Rep Med. 2010;2010. doi: 10.1155/2010/745021. Epub 2010 Sep 1.
We describe a case of the extremely rare entity of myxoglobulosis of the appendix from a 45-year-old white man who was operated urgently with the clinical diagnosis of acute appendicitis. Sectioning of the appendix revealed the presence in the dilated appendiceal lumen of numerous whitish opaque globules ranging in size from 0.2 to 0.7 cm in diameter. A ruptured diverticulum and several smaller ones were also found. On microscopic examination, the globules consisted of faintly eosinophilic laminations of mucin surrounding an amorphous granular core. The mucin was identified by positivity with histochemical mucin stains. After thorough microscopic examination of the appendix, our case was diagnosed as myxoglobulosis due to mucosal hyperplasia, associated with ruptured diverticulum and acellular extra-appendiceal mucin deposits.
我们描述了一例极为罕见的阑尾黏液球蛋白病病例,患者为一名45岁的白人男性,因临床诊断为急性阑尾炎而紧急接受手术。阑尾切片显示,在扩张的阑尾腔内存在大量直径从0.2到0.7厘米不等的白色不透明小球。还发现了一个破裂的憩室和几个较小的憩室。显微镜检查显示,这些小球由围绕无定形颗粒核心的轻度嗜酸性黏液层组成。通过组织化学黏液染色阳性鉴定出黏液。在对阑尾进行全面的显微镜检查后,我们的病例被诊断为黏液球蛋白病,原因是黏膜增生,伴有破裂的憩室和阑尾外无细胞黏液沉积。