Hatanaka Kazuhito, Yoshioka Takako, Tasaki Takashi, Tanimoto Akihide
Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan
Int J Surg Pathol. 2014 Oct;22(7):652-5. doi: 10.1177/1066896913517936. Epub 2014 Jan 7.
Castleman's disease in the pelvic cavity is rare. We present a 72-year-old woman with hyaline vascular type of Castleman's disease of the right ovary. Right ovarian enlargement was detected in the medical examination. Computed tomography revealed a solid mass, measured 2.5 cm in size, in the right ovary. A bilateral salpingo-oophorectomy was performed. Morphologically, lymphoid follicles with regressed germinal centers (GCs) were surrounded by a broad mantle zone composed of concentric rings of small lymphocytes, and the hyalinized blood vessels with plump endothelial cells penetrated radially into GCs. Proliferation of follicular dendritic cells, which were positive for CD21 and epidermal growth factor receptor, were detected in GCs and mantle zone. No other lesions were found. To the best of our knowledge, this is the first case of hyaline vascular type of Castleman's disease of ovarian primary.
盆腔Castleman病罕见。我们报告一例72岁女性,患有右侧卵巢透明血管型Castleman病。体检发现右侧卵巢增大。计算机断层扫描显示右侧卵巢有一个大小为2.5厘米的实性肿块。进行了双侧输卵管卵巢切除术。形态学上,生发中心(GCs)退化的淋巴滤泡被由小淋巴细胞同心环组成的宽阔套区包围,透明化的血管内有丰满的内皮细胞呈放射状穿透进入GCs。在GCs和套区检测到滤泡树突状细胞增殖,其CD21和表皮生长因子受体呈阳性。未发现其他病变。据我们所知,这是首例原发性卵巢透明血管型Castleman病。