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[Effect of Body Mass Index on Outcomes of Mini-ECIRS for Renal Stone]. [体重指数对Mini-ECIRS治疗肾结石结局的影响]。
Q4 Medicine Pub Date : 2025-03-01 DOI: 10.14989/ActaUrolJap_71_3_71
Tetsuo Fukuda, Hiroki Ito, Takahiko Watanabe, Tadashi Tabei, Fukashi Yamamichi, Takaaki Inoue, Kazuki Kobayashi, Junichi Matsuzaki

We retrospectively compared treatment outcomes and complications based on body mass index (BMI) in patients with renal stones treated with mini-endoscopic combined intrarenal surgery (ECIRS) using percutaneous tracts 20 Fr or smaller. Among 1,432 patients who had ECIRS performed at multiple registered facilities between January 2015 and December 2022, 870 patients with renal stones who underwent mini-ECIRS were included after excluding those with anatomical anomalies or incomplete clinical data. The patients were divided into two groups : BMI ≥30 (Group A) and BMI <30 (Group B). The treatment outcomes and complications were compared between the two groups. One month postoperatively, plain computed tomography (CT) and kidney ureter bladder radiography (KUB) were performed to assess stone fragmentation and hydronephrosis. According to postoperative imaging, stone-free was defined as residual fragments 4 mm or less on KUB and 2 mm or less on CT. Of the 870 patients, 86 were in Group A and 784 in Group B. The median (interquartile range) cumulative stone diameter was 33.8 (26.35-50.75) mm in Group A, and 32 (24-47) mm in Group B, respectively. The median operative time was 122.5 (92.25- 166.75) min in Group A and 114.5 (89.75-156) min in Group B. The mean and median (interquartile range) postoperative hospital stay were 5.9±2.5 days and 5 (4-7) days in Group A, and 5.4±3.3 days and 5 (4-6) days in Group B. Stone-free rates were 77.9% (67 cases) by KUB and 61.6% (53 cases) by CT in Group A, and 76.1% (597 cases) by KUB and 58.0% (455 cases) by CT in Group B. The incidence of postoperative fever (≥38.0°C) was 38.4% (33 cases) in Group A and 31.8% (249 cases) in Group B, while septic shock occurred in 2.3% (2 cases) of Group A and 2.6% (20 cases) of Group B. A statistically significant difference (p<0.05) was found in the postoperative hospital stay between the two groups, but no significant differences were observed in the stone-free rates or complication rates. Mini-ECIRS using percutaneous tracts of 20Fr or smaller for renal stones showed no significant difference in SFR and complications between patients with a BMI ≥30 and those with a BMI <30.

我们回顾性比较了采用经皮径径20fr或更小的微型内镜联合肾内手术(ECIRS)治疗肾结石患者的治疗结果和基于体重指数(BMI)的并发症。在2015年1月至2022年12月期间,在多个注册机构进行ECIRS的1432例患者中,在排除解剖异常或临床资料不完整的患者后,纳入了870例接受mini-ECIRS的肾结石患者。将患者分为BMI≥30组(A组)和BMI <30组(B组)。比较两组患者的治疗效果及并发症。术后1个月行计算机断层扫描(CT)和肾输尿管膀胱造影(KUB)评估结石碎裂和肾积水。根据术后影像学,无结石定义为KUB上小于等于4mm, CT上小于等于2mm的残留碎片。870例患者中,A组86例,B组784例。累积结石直径中位数(四分位间距)A组为33.8 (26.35-50.75)mm, B组为32 (24-47)mm。A组中位手术时间122.5 (92.25 ~ 166.75)min, b组中位手术时间114.5 (89.75 ~ 156)min。A组平均和中位(四分位间距)住院时间分别为5.9±2.5天和5 (4 ~ 7)d, b组平均和中位住院时间分别为5.4±3.3天和5 (4 ~ 6)d。A组经KUB检查结石清除率为77.9%(67例),CT检查结石清除率为61.6%(53例)。由KUB和76.1%(597例)和58.0%(455例)的CT在B组术后发热的发生率(≥38.0°C)是38.4%在A组(33例)和31.8%(249例),B组,而脓毒性休克发生在2.3%(2例)组(20例)和2.6%组B一个统计上的显著差异(p < 0.05)被发现在两组间术后住院,但没有观察到显著差异在取石率和并发症发生率。经皮径道20Fr或更小的Mini-ECIRS治疗肾结石,BMI≥30和BMI <30患者的SFR和并发症无显著差异。
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引用次数: 0
[A Case of Radical Nephrectomy that Achieved Complete Remission after Combination Therapy with Pembrolizumab and Lenvatinib for Metastatic Renal Cell Carcinoma]. [1例根治性肾切除术经派姆单抗和Lenvatinib联合治疗转移性肾细胞癌获得完全缓解]。
Q4 Medicine Pub Date : 2025-03-01 DOI: 10.14989/ActaUrolJap_71_3_81
Hitoshi Yokozeki, Takaaki Takuma, Kazuki Kokura, Shoko Uketa, Tomohiro Fukui, Yuichi Uemura, Jun Watanabe

An 81-year-old woman to our hospital complaining of backpain and was diagnosed with a left renal tumor with lung and iliac metastasis. A renal tumor biopsy confirmed clear cell renal cell carcinoma. The patient began combination therapy with pembrolizumab and lenvatinib but experienced fatigue and edema after 1 month. Suspecting cardiac dysfunction induced by Lenvatinib, Lenvatinib was discontinued and treatment with pembrolizumab alone was continued. Three months after treatment initiation, the lung and iliac metastases had resolved, allowing for laparoscopic nephrectomy. Five months post-surgery, no new metastases were detected.

一名81岁妇女来我院主诉背部疼痛,诊断为左肾肿瘤伴肺及髂转移。肾肿瘤活检证实透明细胞肾细胞癌。患者开始使用派姆单抗和lenvatinib联合治疗,但1个月后出现疲劳和水肿。怀疑Lenvatinib引起心功能障碍,停用Lenvatinib,继续单独使用派姆单抗治疗。治疗开始三个月后,肺和髂转移已经消退,允许腹腔镜肾切除术。术后5个月未发现新的转移灶。
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引用次数: 0
[A Case of Paraganglioma of the Spermatic Cord]. 精索副神经节瘤1例。
Q4 Medicine Pub Date : 2025-03-01 DOI: 10.14989/ActaUrolJap_71_3_87
Sayuri Ishibashi, Kotoe Matsuda, Ken Tanaka, Manabu Komine, Koji Kikuchi

A49-year-old man noticed discomfort in the right scrotum and consulted a nearby medical institution. Magnetic resonance imaging revealed a 10 mm tumor in the right spermatic cord, showing low signal intensity on T1-weighted images and high signal intensity on T2-weighted and diffusion-weighted images. Since malignancy could not be ruled out, he was referred to our hospital. Physical examination revealed an elastic, mobile tumor in the right spermatic cord. Ultrasonography showed a solid tumor measuring 10 mm near the right testicle. Although differential diagnoses included lipoma and neurilemmoma, the possibility of malignancy prompted tumor resection. The tumor was a nodular lesion with a clear brown border. Histopathological examination confirmed the diagnosis of paraganglioma. Postoperative metaiodobenzylguanidine scintigraphy, computed tomographic imaging, and hormone testing did not reveal any significant findings, confirming the diagnosis of paraganglioma originating from the spermatic cord.

一名49岁男子发现右阴囊不适,便到附近的医疗机构就诊。磁共振示右侧精索10mm肿瘤,t1低信号,t2及弥散加权高信号。由于不能排除恶性肿瘤,他被转介到我们医院。体格检查显示右侧精索有弹性、可移动的肿瘤。超声检查显示右侧睾丸附近有一个10毫米的实体瘤。虽然鉴别诊断包括脂肪瘤和神经鞘瘤,但恶性肿瘤的可能性促使肿瘤切除。肿瘤为结节状病变,有清晰的棕色边界。组织病理学检查证实副神经节瘤的诊断。术后间十二苄基胍显像、计算机断层成像和激素检测未发现任何显著结果,确认诊断为起源于精索的副神经节瘤。
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引用次数: 0
[A Case of Venous Leiomyosarcoma of the Inferior Vena Cava Diagnosed Preoperatively as an Adrenal Tumor]. [1例下腔静脉平滑肌肉瘤术前诊断为肾上腺肿瘤]。
Q4 Medicine Pub Date : 2025-03-01 DOI: 10.14989/ActaUrolJap_71_3_77
Yushi Miyata, Tomohiro Kanaki, Jumpei Oshima, Takanori Kinjo, Wataru Nakata, Hitoshi Inoue

A 72-year-old woman was referred to our hospital complaining of abdominal pain. Contrast enhanced computed tomography revealed a 53 mm solid tumor with low contrast enhancement on the medial aspect of the right adrenal gland. On magnetic resonance imaging, the tumor showed low signal intensity on T1-weighted images, high signal intensity on T2-weighted images, and high signal intensity on diffusion-weighted images. The patient was diagnosed as having a right adrenal tumor and was referred to our hospital for surgery. Laparoscopic right adrenalectomy was performed. During surgery, we could easily peel the tumor from the adrenal gland, but it was strongly adhered at the inferior vena cava. Considering the possibility of a primary tumor of the inferior vena cava, we converted to open surgery and achieved complete tumor resection by combined partial resection of the inferior vena cava. The cut surface of the tumor was white and firm. Histopathological examination with hematoxylin-eosin staining revealed spindle cell proliferation forming bundle-like structures. Immunohistochemical staining was positive for DESMIN and α-SMA, suggesting leiomyosarcoma. Furthermore, the vascular smooth muscle structure of the resected inferior vena cava was completely replaced by leiomyosarcoma. Therefore, our diagnosis was venous leiomyosarcoma originating from the inferior vena cava. The patient has remained recurrence-free at 21 months after surgery.

一名72岁妇女因腹痛被转诊至我院。增强计算机断层扫描显示在右肾上腺内侧有一个53毫米的实体瘤。在磁共振成像上肿瘤表现为t1加权低信号,t2加权高信号,弥散加权高信号。患者被诊断为右肾上腺肿瘤,并被转介到我院进行手术。行腹腔镜右肾上腺切除术。在手术中,我们可以很容易地从肾上腺上剥离肿瘤,但它在下腔静脉被强烈粘附。考虑到下腔静脉原发肿瘤的可能性,我们改为开放手术,联合部分切除下腔静脉,实现肿瘤完全切除。肿瘤切面白色坚硬。苏木精-伊红染色组织病理学检查显示梭形细胞增生形成束状结构。免疫组化染色DESMIN、α-SMA阳性,提示平滑肌肉瘤。此外,切除的下腔静脉血管平滑肌结构完全被平滑肌肉瘤所取代。因此,我们的诊断是起源于下腔静脉的静脉平滑肌肉瘤。患者术后21个月无复发。
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引用次数: 0
[Penile Fracture in Japan Resulting from a Habit of Over 30 Years Resembling "Taqaandan"]. 【日本30多年“打卡丹”习惯导致阴茎断裂】。
Q4 Medicine Pub Date : 2025-02-01 DOI: 10.14989/ActaUrolJap_71_2_53
Junya Abe, Yutaka Yamashita, Takashi Yoshida, Ko Kobayashi

A 52-year-old man presented to our hospital with penile swelling and pain. The patient was injured when he forcibly bent his erect penis and heard a dull sound different from the"usual click sound"in the morning. His penis was bent dorsally with a hematoma and was purplish red. We diagnosed this as penile fracture and performed surgical treatment. We made a circumferential incision and degloved his penile prepuce. We removed the hematoma and repaired the injured tunica albuginea with absorbable sutures. Urethral injury was not found. He had no complications or erectile dysfunction after surgery. He had the habit of hearing the clicking sound caused by bending his erect penis since he was fifteen years old. This habit seems to resemble the"taqaandan"procedure, which was reported in Kermanshah, Iran. Only 14 penile fractures related to the habit resembling taqaandan have been reported in Japan.

男性,52岁,因阴茎肿痛就诊。患者在早上强行弯曲勃起的阴茎时,听到了一种不同于“通常的咔哒声”的沉闷的声音。他的阴茎背部弯曲,有血肿,呈紫红色。我们诊断为阴茎骨折并进行手术治疗。我们做了一个周身切口,摘掉了他的阴茎包皮。我们切除血肿,用可吸收缝线修复受损的白膜。未发现尿道损伤。术后无并发症或勃起功能障碍。从15岁起,他就习惯听到弯曲勃起的阴茎时发出的咔哒声。这种习惯似乎类似于在伊朗克尔曼沙报道的“taqaandan”程序。据报道,在日本只有14例阴茎骨折与这种类似打卡丹的习惯有关。
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引用次数: 0
[A Rare Case of an Epidermoid Cyst Originating from the Upper Urinary Tract]. [一例罕见的起源于上尿路的表皮样囊肿]。
Q4 Medicine Pub Date : 2025-02-01 DOI: 10.14989/ActaUrolJap_71_2_49
Haruna Ide, Yuji Sakano, Kenichi Kamiya, Kayo Takeuchi, Eiki Hanada, Chul Jang Kim

Epidermoid cysts originating from the upper urinary tract are extremely rare, and only five cases have been reported previously. We report a rare case of epidermoid cyst that originated from the right ureter : A 76-year-old man presented with asymptomatic gross hematuria. Computed tomography showed a right ureteral tumor (14×8 mm in size). Retrograde pyelography showed a defect (14 mm diameter) of the contrast medium in the same region. Urinary cytological examination indicated class III. A ureteral tumor was clinically indicated, and retroperitoneoscopic-assisted radical nephroureterectomy was performed. Postoperative histopathological examination of the resected specimen showed ureteral epidermoid cysts without any malignancy.

起源于上尿路的表皮样囊肿极为罕见,以前仅报道过5例。我们报告一例罕见的起源于右输尿管的表皮样囊肿:一位76岁的男性,表现为无症状的肉眼血尿。计算机断层扫描显示右侧输尿管肿瘤(14×8 mm大小)。逆行肾盂造影显示同一区域造影剂缺陷(直径14 mm)。泌尿细胞学检查为III型。临床表现为输尿管肿瘤,经腹膜后腹腔镜辅助下行根治性肾输尿管切除术。术后病理检查显示输尿管表皮样囊肿,无恶性肿瘤。
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引用次数: 0
[Retroperitoneal Ganglioneuroma with Multifocal Bone Involvement in a Middle-Aged Woman]. [一例中年妇女腹膜后神经节神经瘤伴多灶性骨受累]。
Q4 Medicine Pub Date : 2025-02-01 DOI: 10.14989/ActaUrolJap_71_2_43
Hiroki Watanabe, Hiroaki Kawanishi, Kousuke Kobayashi, Takehiro Yamane, Naoto Takaoka, Yoshiyuki Okada, Takeshi Kubo, Shinji Sumiyoshi, Kazuhiro Okumura

Ganglioneuroma, an infrequent benign tumor that originates from the sympathetic nervous system, is usually a solitary occurrence and rarely occurs at multiple sites. Here, we report a case of retroperitoneal ganglioneuroma with multifocal bone involvement in a middle-aged woman. A 43-year-old female was incidentally diagnosed with a retroperitoneal tumor on abdominal ultrasonography. Contrast-enhanced computed tomography revealed a retroperitoneal tumor that was 11 cm in diameter above her left kidney and multiple bone lesions. Fluorodeoxyglucose positron emission tomography (FDG-PET) showed a slightly high FDG uptake (standardized uptake value (SUV) max, 3.7) in the retroperitoneal mass and mild accumulation in the L1 vertebral body, zygoma, acetabulum, and calcaneus. Biopsies were performed for the retroperitoneal and lumbar spine tumors, both of which were diagnosed as ganglioneuromas. Total surgical resection is the standard treatment of this condition ; however, for this patient, it was difficult to remove all the tumors, and the ganglioneuromas generally followed a benign course. Therefore, a watchful waiting approach was chosen and no tumor growth was observed three years after her first visit to our hospital.

神经节神经瘤是一种罕见的良性肿瘤,起源于交感神经系统,通常是单发的,很少发生在多个部位。在此,我们报告一例中年妇女腹膜后神经节神经瘤伴多灶性骨受累。一位43岁的女性在腹部超声检查中被偶然诊断为腹膜后肿瘤。增强计算机断层扫描显示她的左肾上方有一个直径11厘米的腹膜后肿瘤和多个骨病变。氟脱氧葡萄糖正电子发射断层扫描(FDG- pet)显示腹膜后肿块中FDG摄取稍高(标准化摄取值(SUV)最大值为3.7),L1椎体、颧骨、髋臼和跟骨中有轻度积聚。腹膜后及腰椎肿瘤行活组织检查,均诊断为神经节神经瘤。全手术切除是治疗此病的标准方法;然而,对于该患者,肿瘤很难全部切除,神经节神经瘤一般呈良性发展。因此,我们选择了观察等待的方式,在她第一次来我院就诊3年后,没有发现肿瘤的生长。
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引用次数: 0
[The Introduction of Pubic Hair into the Bladder : A Possibility of an Alternate Mechanism]. [阴毛进入膀胱:一种可能的替代机制]。
Q4 Medicine Pub Date : 2025-01-01 DOI: 10.14989/ActaUrolJap_71_1_1
Koji Koizumi

In patients with an indwelling Foley catheter, pubic hair may be introduced into the bladder. This is believed to occur because the pubic hairs are pushed into the bladder during catheter replacement. However, compared withpatients on intermittent self-catheterization, patients withan indwelling Foley catheter have fewer chances of their pubic hair being pushed into the bladder. This suggests the presence of an alternate mechanism responsible for introducing pubic hair into the bladder during catheter replacement. We performed several experiments to identify this. In a urethral model created with a silicone tube and Foley catheter, a pubic hair was placed between the tube and catheter, and the catheter was moved forward and backward. We confirmed that the pubic hair moved only toward the hair root side. This motion was assumed to be the mechanism by which pubic hair is introduced into the bladder.

留置Foley导尿管的患者,阴毛可能会进入膀胱。这被认为是由于在更换导尿管时阴毛被推入膀胱。然而,与间歇性自我导尿的患者相比,留置Foley导尿的患者阴毛被推入膀胱的机会更少。这表明存在一种替代机制,负责在导管置换期间将阴毛引入膀胱。我们做了几个实验来确认这一点。在用硅胶管和Foley导尿管制作的尿道模型中,在管和导尿管之间放置一根阴毛,并向前和向后移动导尿管。我们确认阴毛只向发根一侧移动。这种运动被认为是阴毛进入膀胱的机制。
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引用次数: 0
[A Case of Metastatic Testicular Cancer after Kidney Transplantation in which Complete Remission was Achieved]. 【肾移植后转移性睾丸癌完全缓解1例】。
Q4 Medicine Pub Date : 2025-01-01 DOI: 10.14989/ActaUrolJap_71_1_9
Ojiro Tokairin, Takashige Abe, Kiyohiko Hotta, Daiki Iwami, Tatsu Tanabe, Takahiro Osawa, Ryuji Matsumoto, Takayuki Hirose, Hiroshi Kikuchi, Haruka Miyata, Naoya Iwahara, Shuhei Yamada, Nobuo Shinohara

We report a case of testicular cancer after kidney transplantation in a 29-year-old man. Twenty-two years after the surgery, computed tomography (CT) showed a retroperitoneal mass 3 cm in diameter. Positron emission tomography (PET) -CT revealed high FDG uptake in both the right testis and retroperitoneal mass. Regarding serum tumor markers, α fetoprotein (AFP) was slightly elevated to 12.5 ng/ml. He underwent right radical orchiectomy, and pathological examination revealed pure seminoma. After surgery, the serum AFP level remained high (12. 9 ng/ml), and we initially considered this nonseminoma patient to have a good prognosis according to International Germ Cell Consensus Classification. During three cycles of a combination regimen including bleomycin, etoposide, and cisplatin (BEP), we performed adjustment of immunosuppressive therapy, treatment for Cytomegalovirus infection (valganciclovir hydrochloride), and that for other adverse events associated with systemic chemotherapy. The chemotherapy schedule was delayed, and bleomycin (third course, day 15) was skipped due to adverse effects. After 3 cycles of BEP, the retroperitoneal lymph node metastasis shrunk from 3.0 to 1.5 cm in diameter. In contrast to the good radiological response, the serum AFP level gradually increased during the treatment to 102.6 ng/ml. Therefore, we did not consider the AFP elevation to have derived from residual cancer, and decided to perform close follow-up. During the 3-year follow-up, AFP decreased to around 20 ng/ml, and PET-CT did not show any uptake in the retroperitoneal mass or other sites.

我们报告一例29岁男性肾移植后睾丸癌的病例。手术22年后,计算机断层扫描(CT)显示一个直径3厘米的腹膜后肿块。正电子发射断层扫描(PET) -CT显示右侧睾丸和腹膜后肿块的高FDG摄取。血清肿瘤标志物α胎蛋白(AFP)略升高至12.5 ng/ml。行右侧根治性睾丸切除术,病理检查显示为纯精原细胞瘤。术后血清甲胎蛋白水平维持在较高水平(12。9 ng/ml),根据国际生殖细胞共识分类,我们最初认为该非精原细胞瘤患者预后良好。在包括博来霉素、依托泊苷和顺铂(BEP)的三个周期的联合治疗方案中,我们调整了免疫抑制治疗、巨细胞病毒感染治疗(盐酸缬更昔洛韦)以及与全身化疗相关的其他不良事件。化疗计划推迟,博莱霉素(第三疗程,第15天)因不良反应而被跳过。经3个周期的BEP治疗后,腹膜后淋巴结转移灶直径由3.0 cm缩小至1.5 cm。与良好的放射学反应相反,治疗期间血清AFP水平逐渐升高至102.6 ng/ml。因此,我们不认为AFP升高来源于残留癌,并决定进行密切随访。随访3年,AFP降至20 ng/ml左右,PET-CT未见腹膜后肿块及其他部位摄取。
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引用次数: 0
[A Case of Pelvic Arteriovenous Malformation in a Male with Massive Bladder Bleeding which Caused Severe Hemorrhagic Hypovolemic Shock]. [1例男性膀胱大出血并发骨盆动静脉畸形致严重出血性低血容量性休克]。
Q4 Medicine Pub Date : 2025-01-01 DOI: 10.14989/ActaUrolJap_71_1_17
Takuro Miyagawa, Yuki Kita, Naoya Kani, Wataru Tanaka, Takahiro Yamaguchi, Yusuke Hama, Kyohei Sugiyama, Ryo Iguchi, Naoto Terai, Koji Inoue

Congenital arteriovenous malformation (AVM) in the male pelvis is extremely rare. We present a case of this disease with massive bladder bleeding which caused severe hemorrhagic shock. Diagnosis of pelvic AVM was confirmed by computed tomography and angiography. He was treated with transcatheter arterial embolization of the bilateral internal iliac arteries. We discuss the clinical course and the treatment for AVM in this case, and review the literature.

先天性动静脉畸形(AVM)在男性骨盆是非常罕见的。我们报告一例因膀胱大量出血而引起严重失血性休克的病例。通过计算机断层扫描和血管造影证实盆腔AVM的诊断。他接受了双侧髂内动脉经导管栓塞治疗。我们讨论该病例的临床过程和治疗方法,并复习文献。#农协。
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引用次数: 0
期刊
Acta Urologica Japonica
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