Bracale Umberto, Pacelli Francesco, Milone Marco, Bracale Umberto Marcello, Sodo Maurizio, Merola Giovanni, Troiani Teresa, Di Salvo Enrico
Department of Surgical Specialities and Nefrology, University "Federico II" of Naples, Via Pansini, 5, Naples, 80100, Italy.
Department of Clinical and Experimental Medicine 'F. Magrassi', Second University of Naples, Naples, Italy.
BMC Surg. 2017 Apr 12;17(1):38. doi: 10.1186/s12893-017-0238-6.
Castleman's disease is a rare lymphoproliferative disorder of unknown etiology that most commonly presents as a mediastinal nodal mass. It is exceptionally uncommon for Castleman's disease to present in the mesentery and, only 53 cases have ever been described in the literature. Standard treatment for this lymphoproliferative disorder involving a single node is a complete "en bloc" surgical resection which has proven to be a curative approach in almost all cases without recurrence after 20 years of follow up. All 53 reported cases of mesenteric Castleman's disease, except one, were treated with laparotomy.
We report on a case of mesenteric Castleman's disease localized in the mesentery which is the second reported case if its kind and was treated by a laparoscopic-assisted procedure. Our female patient had an uneventful postoperative course and was discharged in the 5 post-operative day. No signs of recurrence were present as evidenced by physical examination and total body CT scan 24 months after the operation. We compare our case with the other reported cases in which Castleman's disease presented as an isolated mass in the abdomen.
Although a rare disease, Unicentric Castleman's disease should always be considered when a solid asymptomatic abdominal mass is occasionally presented. The laparoscopic approach (LA) allows for the achievement of better results than open surgery, including a reduction in postoperative pain and length of hospital stay. In cases of masses of an uncertain nature, LA must be considered the last diagnostic tool and the first treatment one.
卡斯特曼病是一种病因不明的罕见淋巴增生性疾病,最常见的表现是纵隔淋巴结肿块。卡斯特曼病出现在肠系膜的情况极为罕见,文献中仅描述过53例。对于这种累及单个淋巴结的淋巴增生性疾病,标准治疗方法是完整的“整块”手术切除,事实证明,这在几乎所有病例中都是一种治愈性方法,随访20年后无复发。除1例之外,所有53例报告的肠系膜卡斯特曼病病例均接受了剖腹手术治疗。
我们报告1例位于肠系膜的肠系膜卡斯特曼病病例,这是该类型的第二例报告病例,采用腹腔镜辅助手术进行治疗。我们的女性患者术后恢复顺利,术后第5天出院。术后24个月的体格检查和全身CT扫描均未发现复发迹象。我们将我们的病例与其他报告的卡斯特曼病表现为腹部孤立肿块的病例进行了比较。
尽管是罕见疾病,但当偶尔出现无症状实性腹部肿块时,应始终考虑单中心卡斯特曼病。腹腔镜手术(LA)比开放手术能取得更好的效果,包括减轻术后疼痛和缩短住院时间。对于性质不确定的肿块病例,LA必须被视为最后的诊断工具和首选的治疗方法。