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以不寻常的盆腔腹膜后肿块为表现的Castleman病

Castleman's Disease Presenting as an Unusual Pelvic Retroperitoneal Mass.

作者信息

Patil Mallikarjun B, Sindgikar Vikram U, Kulkarni Sai, Biradar Dayanand, Siddesh Ashwin

机构信息

General Surgery, Shri B. M. Patil Medical College Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, IND.

Pathology, Shri B. M. Patil Medical College Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, IND.

出版信息

Cureus. 2024 Oct 23;16(10):e72196. doi: 10.7759/cureus.72196. eCollection 2024 Oct.

Abstract

Castleman's disease (CD) is characterised by benign lymphoepithelial proliferation and is a peculiar form of angiofollicular lymph node hyperplasia rather than a neoplasm or a hamartoma. CD is broadly classified as unicentric CD (UCD) and multicentric CD. In the unicentric variant, patients have localised disease affecting only a single lymph node or a group of adjacent nodes in a single region, which clinically presents as an enlarging mass without any other significant symptoms. The mediastinum and thoracic lymph nodes are commonly involved. However, it is uncommon for CD to occur in the pelvic presacral region of the retroperitoneum. A 31-year-old male presented with progressive, dull aching, intermittent lower abdomen pain for three months with no aggravating or relieving factors or any associated symptoms. He was haemodynamically stable, and his general physical examination was normal. An abdominal examination elicited mild tenderness in the left iliac region of the abdomen. Contrast-enhanced computed tomography of the abdomen and pelvis revealed an encapsulated nodal mass with intralesional calcification displacing the bladder to the right side, and fine needle aspiration cytology showed atypical cells. An exploratory laparotomy was performed with an in toto excision biopsy of the pelvic retroperitoneal mass, and it was diagnosed as a hyaline-vascular variant of UCD. Immunohistochemistry revealed angiofollicular hyperplasia and atretic germinal centres that are crossed by sclerotic vessels and hyalinisation, confirming the diagnosis. The patient is currently asymptomatic and is leading a routine life. The hyaline-vascular variant is the most common variant seen in UCD. Compared to the multicentric type, the unicentric type seldom exhibits systemic involvement. Surgical resection is typically curative. Although it is asymptomatic, it is essential to achieve complete surgical resection to prevent the neoplastic potentialities of CD. In the presence of an uncertain solitary solid pelvic retroperitoneal mass, the diagnosis of UCD should be considered, as surgical resection can achieve a favourable outcome.

摘要

Castleman病(CD)的特征为良性淋巴上皮增生,是血管滤泡性淋巴结增生的一种特殊形式,而非肿瘤或错构瘤。CD大致分为单中心性CD(UCD)和多中心性CD。在单中心性变体中,患者患有局限性疾病,仅影响单个区域的单个淋巴结或一组相邻淋巴结,临床上表现为肿块逐渐增大,无任何其他明显症状。纵隔和胸部淋巴结常受累。然而,CD发生于腹膜后盆腔骶前区域并不常见。一名31岁男性出现进行性、钝痛、间歇性下腹部疼痛3个月,无加重或缓解因素,也无任何相关症状。他血流动力学稳定,全身体格检查正常。腹部检查发现腹部左髂区有轻度压痛。腹部和盆腔增强计算机断层扫描显示一个有包膜的结节性肿块,病灶内有钙化,将膀胱推向右方,细针穿刺细胞学检查显示非典型细胞。进行了剖腹探查术,对盆腔腹膜后肿块进行了完整切除活检,诊断为UCD的透明血管变体。免疫组织化学显示血管滤泡增生和闭锁的生发中心,有硬化血管和玻璃样变穿过,证实了诊断。患者目前无症状,过着正常生活。透明血管变体是UCD中最常见的变体。与多中心型相比,单中心型很少表现出全身受累。手术切除通常可治愈。尽管无症状,但为防止CD的肿瘤潜能,实现完整的手术切除至关重要。在存在不确定的孤立性盆腔腹膜后实性肿块时,应考虑UCD的诊断,因为手术切除可取得良好结果。

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