Castleman病。老年患者腹膜后肿瘤定位的罕见临床病例

Q4 Immunology and Microbiology Acta Biomedica Scientifica Pub Date : 2023-07-11 DOI:10.29413/abs.2023-8.3.14
M. B. Polyanskiy, I. N. Zvyagin, V. A. Petrik, M. V. Temirbulatov
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引用次数: 0

摘要

Castleman病是一种极其罕见的淋巴系统良性疾病,估计发病率为1-9例/ 1,000,000。其病因尚不清楚;白细胞介素6 (IL-6)在发病机制中起重要作用。Castleman病有两种临床形式:局部(高达90%的病例),预后良好,主要通过手术方法治疗;全身性(高达10%的病例)预后较差,采用药物治疗。诊断很少在术前阶段确定。的目标。目的:报道一例罕见的外源性Castleman肿瘤的诊断和治疗。一位66岁的患者住进了ge Ostroverkhov Kursk肿瘤科学和临床中心的腹部肿瘤科。诊断:预防检查发现右侧腹膜后肿块;超声及CT未见外周淋巴结病变。经检查,初步诊断:小肠肠系膜胃肠道间质瘤(GIST)。根据病例会议的结果,决定进行手术-气管内麻醉下腹腔镜切除肿瘤。对于手术入路,选择扇形排列的端口。手术没有并发症。术中出血量50.0 ml,总手术时间98 min。根据组织学研究结果,诊断如下:Castleman病,单中心型,透明血管变异。整体手术是治疗局限性Castleman病的标准方法。在所有病例中,长期随访显示几乎所有患者都有较长的无复发期。随访检查(腹腔及腹膜后间隙超声、腹腔增强CT、胸部CT),观察年内未见疾病复发。Castleman病是一种罕见的病因不明的非克隆性淋巴细胞增生性疾病。一个罕见的腹膜后定位病例表明,在腹膜肿块性质不确定的病例中,Castleman病应包括在鉴别诊断中。
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Castleman disease. A rare clinical case of retroperitoneal tumor localization in an elderly patient
Castleman disease is an extremely rare benign disease of the lymphatic system with an estimated incidence of 1–9 cases per 1,000,000. Its etiology remains unknown; interleukin 6 (IL-6) plays an important role in pathogenesis. Castleman disease has two clinical forms: localized (up to 90 % of cases) with a favorable prognosis, treated predominantly by surgical method; generalized (up to 10 % of cases) with less favorable prognosis, treated by pharmacological therapy. The diagnosis is rarely established at the preoperative stage.The aim. To present a clinical case of diagnosis and treatment of Castleman tumor of a rare topical localization.Results. A 66-year-old patient was admitted at the Abdominal Oncology Department of the G.E. Ostroverkhov Kursk Oncology Scientific and Clinical Center.Diagnosis: Retroperitoneal mass on the right found at the preventive examination; no peripheral lymphadenopathy was detected on ultrasound and computed tomography (CT). After the examination, a preliminary diagnosis was made: Gastrointestinal stromal tumor (GIST) of the small intestine mesentery.  Based on the results of the case conference, the decision was taken to perform a surgery – laparoscopic removal of the tumor under endotracheal anesthesia. For surgical approach, a fan-shaped arrangement of ports was chosen. The surgery had no complications. Intraoperative blood loss was 50.0 ml. The total operating time was 98 minutes.According to the results of the histological study, the following diagnosis was made: Castleman disease, unicentric form, hyaline-vascular variant. En bloc surgery is the standard method for the treatment of localized forms of the Castleman disease. In all cases, long-term follow-up shows a long relapse-free period in almost all patients.During follow-up examinations (ultrasound of the abdominal cavity and retroperitoneal space, CT of the abdominal cavity with contrast enhancement, CT of the chest), no disease recurrence was detected during the year of observation.Castleman disease is a rare non-clonal lymphoproliferative disease of unknown etiology. A rare case of its retroperitoneal localization indicates that in cases with an uncertain nature of the peritoneal mass, Castleman disease should be included in the differential diagnostic search.
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来源期刊
Acta Biomedica Scientifica
Acta Biomedica Scientifica Immunology and Microbiology-General Immunology and Microbiology
CiteScore
0.40
自引率
0.00%
发文量
106
审稿时长
7 weeks
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