Arai Takumi, Obinata Daisuke, Ohashi Kazuki, Inagaki Yuki, Hashimoto Sho, Nakahara Ken, Yoshizawa Tsuyoshi, Mochida Junichi, Takahashi Satoru
Department of Urology, Nihon University School of Medicine, Tokyo, Japan.
Medicine (Baltimore). 2025 Jul 25;104(30):e43622. doi: 10.1097/MD.0000000000043622.
Penile metastasis from renal cell carcinoma (RCC) is an extremely rare clinical entity, particularly in the era of immune-checkpoint inhibitor and tyrosine-kinase inhibitor combination therapy. The mechanisms, clinical presentation, and optimal management of such cases remain poorly understood.
A 75-year-old man with metastatic RCC undergoing systemic therapy developed persistent, painful erections (malignant priapism), along with urinary retention, general malaise, and back pain, 2 years after initiating treatment.
Magnetic resonance imaging of the penis revealed a hypointense lesion on T2-weighted imaging and restricted diffusion on diffusion-weighted imaging, suggestive of tumor infiltration into the corpus cavernosum. Blood gas analysis from corporal aspiration was consistent with nonischemic priapism. A diagnosis of penile metastasis from RCC was established.
Embolization of the common penile artery was performed, followed by palliative radiotherapy (30 gray in 10 fractions).
Despite these interventions, penile rigidity persisted, though partial symptomatic relief and pain reduction were achieved. Disease progression was noted, and the patient died approximately 3 months after the diagnosis of penile metastasis.
This is the first reported case of penile metastasis from RCC during immune-checkpoint inhibitor-tyrosine-kinase inhibitor therapy, highlighting a rare but clinically important metastatic pattern potentially unmasked by prolonged survival. Retrograde dissemination via Batson venous plexus may underlie this presentation. Radiotherapy and embolization may offer partial symptomatic relief, but the prognosis remains poor. Accumulation of further cases is necessary to guide future management strategies.
肾细胞癌(RCC)的阴茎转移是一种极其罕见的临床情况,尤其是在免疫检查点抑制剂和酪氨酸激酶抑制剂联合治疗的时代。此类病例的机制、临床表现和最佳治疗方法仍知之甚少。
一名75岁患有转移性RCC且正在接受全身治疗的男性,在开始治疗2年后出现持续性、疼痛性勃起(恶性阴茎异常勃起),伴有尿潴留、全身不适和背痛。
阴茎磁共振成像显示T2加权成像上有一个低信号病变,扩散加权成像上有扩散受限,提示肿瘤浸润到海绵体。阴茎穿刺血气分析与非缺血性阴茎异常勃起一致。确诊为RCC阴茎转移。
对阴茎总动脉进行栓塞,随后进行姑息性放疗(10次分割,共30格雷)。
尽管采取了这些干预措施,阴茎僵硬仍然存在,不过症状部分缓解,疼痛减轻。疾病出现进展,患者在诊断为阴茎转移后约3个月死亡。
这是免疫检查点抑制剂 - 酪氨酸激酶抑制剂治疗期间首例报道的RCC阴茎转移病例,突出了一种罕见但临床上重要的转移模式,可能因生存期延长而显现。通过巴特森静脉丛的逆行播散可能是此表现的基础。放疗和栓塞可能会提供部分症状缓解,但预后仍然很差。需要积累更多病例以指导未来的治疗策略。