Apostolski Duje, Roitner Florian
Department of Internal Medicine, Hospital St. Josef Braunau, Braunau am Inn, Austria.
Cancer Rep (Hoboken). 2024 Dec;7(12):e70077. doi: 10.1002/cnr2.70077.
Metastatic disease of a urinary bladder cancer localized in the upper abdomen is very rare. This case report describes the first patient with a urinary bladder cancer progression, initially presenting as a gastric outlet obstruction due to peritoneal carcinomatosis.
We present the case of a 78-years-old male patient who was admitted to Hospital St. Josef Braunau in Austria with persistent vomiting. In the medical history, the most prominent finding was a diagnosed high-risk NMIBC. At the time, patient was between 2. and 3. BCG maintenance instillation cycle, following two transurethral resections. Routine follow-up cystoscopy 1 month before admission to our department showed no evidence of disease recurrence. Due to the therapy resistant vomiting, gastroscopy was performed, revealing duodenal stenosis without mucosal changes. Subsequently performed abdominal CT-scan showed homogenous swelling of the mesenteric fat tissue around duodenum, spreading retroperitoneal to both kidneys. In the absence of the typical peritoneal carcinomatosis features, the finding was firstly described as an inflammation of mesenteric fat or panniculitis mesenterialis. Further deterioration of patient's condition and later occurred bilateral hydronephrosis raised a suspicion of peritoneal carcinomatosis. Consequently, conducted laparoscopic exploration confirmed the suspicion describing the tissue conglomerate typical for peritoneal carcinomatosis surrounding the duodenum. Pathohistological analysis of taken samples proved urothelial cancer cells, confirming the diagnosis of metastatic bladder cancer disease.
This case report presents a very unusual presentation of metastatic urinary bladder cancer that could help clinicians to consider this diagnosis when encountering similar clinical features.
膀胱癌转移至上腹部极为罕见。本病例报告描述了首例膀胱癌进展患者,最初表现为因腹膜癌病导致的胃出口梗阻。
我们报告一例78岁男性患者,因持续性呕吐入住奥地利圣约瑟夫布劳瑙医院。病史中最突出的发现是诊断为高危非肌层浸润性膀胱癌。当时,患者在接受两次经尿道切除术后,正处于卡介苗维持灌注的第2至3个周期。入院前1个月的常规随访膀胱镜检查未发现疾病复发迹象。由于治疗抵抗性呕吐,进行了胃镜检查,发现十二指肠狭窄但无黏膜改变。随后进行的腹部CT扫描显示十二指肠周围肠系膜脂肪组织均匀肿胀,向后腹膜扩散至双肾。由于缺乏典型的腹膜癌病特征,该发现最初被描述为肠系膜脂肪炎症或肠系膜脂膜炎。患者病情进一步恶化,随后出现双侧肾积水,这引发了对腹膜癌病的怀疑。因此,进行的腹腔镜探查证实了怀疑,描述了十二指肠周围典型的腹膜癌病组织团块。所取样本的病理组织学分析证实为尿路上皮癌细胞,确诊为转移性膀胱癌。
本病例报告展示了转移性膀胱癌一种非常不寻常的表现,这有助于临床医生在遇到类似临床特征时考虑该诊断。