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首页> 外文期刊>Pathologica >Extracutaneous seborrheic inclusion cyst: an unusual presentation.
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Extracutaneous seborrheic inclusion cyst: an unusual presentation.

机译:皮外脂溢性囊肿:异常表现。

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Seborrheic inclusion cyst is an unusual variant of epidermal cyst characterized by parietal histology similar to seborrheic keratosis. Cysts with such changes have been called "seborrheic keratosis-like changes in epidermal cyst" or epidermoid cyst with seborrheic verruca-like cyst wall cyst". To date, this lesion has been described exclusively in cutaneous sites. We describe the first case of an extracutaneous seborrheic inclusion cyst arising from round ligament. A 30-year-old female was referred to our institution for abdominal pain. Ultrasonography showed a hypoechoic heterogeneous, round mass adjacent to the lower extremity of the left ovary, measuring 4.5 cm in maximum diameter. Contrast-enhanced computed tomography of the pelvis in the venous phase showed a round (4.5 cm in diameter) cystic lesion with inhomogeneous fluid content in the side of the left large ligament and anterior to the homolateral adnexa. Laparoscopic resection of the mass was performed. Intraoperatively, an extraperitoneal glistening pelvic mass was discovered: the lesion was attached to the intrapelvic 1/3 middle portion of the left round ligament. Macroscopically, the mass measured 6 cm x 6 cm x 3.5 cm and exhibited a smooth and glistening external surface. On cut sections, the mass was an unilocular cyst filled with soft, yellow, amorphous material. Histologically, the cystic wall was lined by a stratified squamous epithelium with a granular cell layer. The cavity contained keratin-like material. The cystic wall showed numerous areas with close-set basaloid cells and pseudohorn cysts. The latter aspect consisted of cystic invaginations of the epithelium filled with surface keratin, which in a given microscopic section may be cut in cross-section, thereby appeared as "cysts" within the involved epithelium. Parietal rupture was present, accompanied by granulomatous inflammation. There were no postoperative complications, and the patient was discharged 3 days after the procedure. The present case is unique in that it is the first reported case of an extracutaneous seborrheic inclusion cyst arising from a very unusual site, namely the round ligament. The site of origin of the lesion and its cystic nature were established by computed tomography findings. Conservative treatment with enbloc resection was possible. Histological examination confirmed computed tomography findings. The present report described a lesion typically found in dermatopathology practice, but which had arisen in an extracutaneous site.
机译:脂溢性包涵囊肿是表皮囊肿的不寻常变体,其特征在于壁组织学类似于脂溢性角化病。具有这种变化的囊肿被称为“脂溢性角化病样变化的表皮囊肿”或“表皮样囊肿伴脂溢性疣状囊肿壁囊肿”。迄今为止,该病灶仅在皮肤部位进行了描述。圆韧带引起的皮脂溢性囊外皮囊肿,一名30岁女性因腹痛转诊至我们的机构,超声检查显示低回声异质圆形肿块,邻近左卵巢下肢,最大直径为4.5厘米。盆腔静脉造影造影增强检查显示,圆形大胆囊性病变(直径4.5厘米)在左大韧带一侧和同侧附件前侧具有不均匀的液体含量,并进行腹腔镜切除肿块。术中发现腹膜外闪耀的骨盆肿块:病变附着在左圆形骨盆内1/3中段服装。宏观上,该质量为6cm×6cm×3.5cm,并显示出光滑和闪闪发光的外表面。在切开的切片上,肿块是充满软的,黄色的无定形物质的单眼囊肿。组织学上,囊性壁被分层的鳞状上皮和颗粒细胞层所衬。空腔包含角蛋白样物质。囊壁显示出许多区域,基底细胞密闭,假角囊肿。后一个方面由充满表面角蛋白的上皮的囊性内陷组成,其在给定的显微切片中可以被切开横截面,从而在所涉及的上皮内表现为“囊肿”。存在顶壁破裂,并伴有肉芽肿性炎症。没有术后并发症,手术后3天出院。本例的独特之处在于,这是首次报道的皮脂溢性囊肿囊肿,是由非常罕见的部位(即圆形韧带)引起的。病变的起源部位及其囊性是通过计算机断层扫描发现的。整体切除的保守治疗是可能的。组织学检查证实了计算机断层扫描的发现。本报告描述了通常在皮肤病理学实践中发现但在皮外部位出现的病变。

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