Sugimoto Hiroshi, Sugimoto Keisuke, Inoue Haruna, Tanaka Ryuichiro, Nakata Kyosuke, Okino Takeshi, Kinoshita Yoshihisa, Kajimoto Kazuhiro
Department of Respiratory Medicine, Kobe Red Cross Hospital, Kobe, Japan.
Department of Pathology, Kobe Red Cross Hospital, Kobe, Japan.
Respir Med Case Rep. 2021 Jan 19;32:101348. doi: 10.1016/j.rmcr.2021.101348. eCollection 2021.
Pulmonary lymphangitic carcinomatosis (PLC) is a metastatic lung disease of malignant tumors that spread through pulmonary lymphatic vessels. Although prompt diagnosis and specific treatment of PLC are required due to the poor prognosis associated with this disease, it is often challenging to determine the primary cancer site.
A 67-year-old Japanese woman presented to our hospital with a 10-day history of cough and dyspnea on exertion. Chest radiography and computed tomography (CT) revealed diffuse nodular opacities with interlobular septal thickening. Both bronchoalveolar lavage (BAL) and transbronchial lung biopsy (TBLB) revealed carcinoma cells with unknown origin. Contrast-enhanced CT depicted a mass in the right ureter with hydronephrosis, and retrograde urography showed a narrowing of the right ureter. Urine cytology from her right ureter via ureteral catheter also revealed atypical cells, highly suggestive of malignancy. Immunohistochemical examination of lung specimens via TBLB showed results consistent with lung metastasis of ureteral cancer. Therefore, we arrived at a diagnosis of PLC secondary to ureteral cancer.
This case encouraged multidisciplinary discussion and a whole-body examination, including TBLB with immunohistochemistry, to determine the origin of PLC.
肺淋巴管癌病(PLC)是一种恶性肿瘤的转移性肺部疾病,通过肺淋巴管扩散。尽管由于该疾病预后较差,需要对PLC进行及时诊断和特异性治疗,但确定原发癌部位往往具有挑战性。
一名67岁的日本女性因咳嗽和劳力性呼吸困难10天前来我院就诊。胸部X线和计算机断层扫描(CT)显示弥漫性结节状混浊伴小叶间隔增厚。支气管肺泡灌洗(BAL)和经支气管肺活检(TBLB)均发现来源不明的癌细胞。增强CT显示右侧输尿管有肿块伴肾积水,逆行尿路造影显示右侧输尿管狭窄。通过输尿管导管对其右侧输尿管进行尿液细胞学检查也发现非典型细胞,高度提示恶性肿瘤。经TBLB对肺标本进行免疫组织化学检查,结果与输尿管癌肺转移一致。因此,我们诊断为继发于输尿管癌的PLC。
该病例促使进行多学科讨论和全身检查,包括带免疫组织化学的TBLB,以确定PLC的起源。