Gazzah Wael, Mzoughi Mahdy, Lahouar Rayen, Benkhalifa Badreddine, Zaidi Bacem, Salem Braiek
University of Sousse, faculty of Medicine, Department of Urology, Ibn El Jazzar Hospital, Kairouan, Tunisia.
University of Sousse, faculty of Medicine, Department of Urology, Ibn El Jazzar Hospital, Kairouan, Tunisia.
Int J Surg Case Rep. 2024 Jul;120:109887. doi: 10.1016/j.ijscr.2024.109887. Epub 2024 Jun 6.
Primary adenocarcinoma of the renal pelvis is a rare and unique malignancy, representing a small fraction of renal cancers and posing significant diagnostic challenges due to its unusual presentation and similarity in symptoms to more common excretory tract disorders. This case emphasizes the importance of distinguishing this pathology from other renal neoplasms and metastatic adenocarcinomas that originate in the digestive tract.
We report the case of a 34-year-old man with no significant medical history who presented persistent lower back pain but no hematuria, which is atypical for renal pathologies. Initial imaging identified a 30 × 14 mm enhancement mass in the right renal pelvis. Surgical intervention was performed through right nephroureterectomy, including excision of the bladder cuff. Histopathological examination confirmed the diagnosis of primary intestinal-type adenocarcinoma of the renal pelvis, characterized by necrotic carcinomatous proliferation with varying architectural patterns and occasional signet ring cells.
The diagnosis of primary renal pelvis adenocarcinoma is complicated by its nonspecific symptomatology and the potential for misdiagnosis as a more common urothelial carcinoma or a metastatic digestive-origin adenocarcinoma. Immunohistochemical staining supported a primary rather than metastatic digestive tract origin. This case underscores the need for a comprehensive diagnostic approach, including advanced imaging and meticulous histopathological analysis, to effectively differentiate this rare entity from other neoplasms.
This case highlights the diagnostic complexities and the critical need to be aware among clinicians about rare renal cancers such as primary adenocarcinoma of the renal pelvis. It also stresses the importance of interdisciplinary collaboration in the diagnosis and management of such rare cases, improving our understanding and requiring timely and accurate treatment.
肾盂原发性腺癌是一种罕见且独特的恶性肿瘤,在肾癌中占比很小,因其表现不寻常且症状与更常见的泌尿道疾病相似,给诊断带来了重大挑战。本病例强调了将这种病理类型与其他肾肿瘤以及起源于消化道的转移性腺癌相区分的重要性。
我们报告一例34岁男性患者,既往无重大病史,出现持续性下背部疼痛但无血尿,这在肾脏疾病中并不典型。初始影像学检查发现右肾盂有一个30×14毫米的强化肿块。通过右肾输尿管切除术进行了手术干预,包括切除膀胱袖口。组织病理学检查确诊为肾盂原发性肠型腺癌,其特征为坏死性癌性增殖,具有不同的结构模式,偶见印戒细胞。
肾盂原发性腺癌的诊断因症状不具特异性且可能被误诊为更常见的尿路上皮癌或转移性消化道起源腺癌而变得复杂。免疫组化染色支持其起源于原发性而非转移性消化道。本病例强调了需要一种全面的诊断方法,包括先进的影像学检查和细致的组织病理学分析,以有效地区分这种罕见实体与其他肿瘤。
本病例突出了诊断的复杂性以及临床医生了解诸如肾盂原发性腺癌等罕见肾癌的迫切需求。它还强调了跨学科协作在诊断和管理此类罕见病例中的重要性,增进了我们的理解并要求及时准确的治疗。