Kashima Hirotaka, Minami Ryuki, Ozawa Tomomi, Matsumoto Atsushi, Kimura Yuto, Takeda Yasuhiro, Ueo Taro, Okano Akihiro, Kusumi Fusako, Ohana Masaya
Department of Gastroenterology, Tenri Hospital.
Nihon Shokakibyo Gakkai Zasshi. 2022;119(3):259-266. doi: 10.11405/nisshoshi.119.259.
A 57-year-old male patient with unresectable pancreatic head cancer was treated with chemotherapy, 5 courses of gemcitabine plus nab paclitaxel therapy, and 9 courses of gemcitabine monotherapy. After 12 months of treatment, he was admitted to our hospital with headache and dyspnea. He was diagnosed with gemcitabine-induced thrombotic microangiopathy (TMA) due to acute kidney dysfunction, hemolytic anemia, and thrombocytopenia. Gemcitabine was discontinued, and symptoms were improved without using hemodialysis and plasma exchange. After his renal function recovered, we started S-1 chemotherapy. Eighteen months later, the patient was alive. Looking back, we realized that fragment red blood cells appeared in complete blood count and serum LDH elevated at 5 months prior to admission, serum creatinine level increased slowly at 4 months prior to admission, and blood pressure elevated significantly at 2 months prior to admission. Therefore, physicians must be aware of TMA as a possible adverse event to gemcitabine. As in this case, hemolytic findings and hypertension in patients treated with gemcitabine may help early detection of TMA.
一名57岁的男性不可切除性胰头癌患者接受了化疗,包括5个疗程的吉西他滨联合白蛋白结合型紫杉醇治疗以及9个疗程的吉西他滨单药治疗。治疗12个月后,他因头痛和呼吸困难入院。由于急性肾功能不全、溶血性贫血和血小板减少,他被诊断为吉西他滨诱导的血栓性微血管病(TMA)。停用吉西他滨后,未进行血液透析和血浆置换,症状得到改善。肾功能恢复后,我们开始了S-1化疗。18个月后,患者仍然存活。回顾发现,入院前5个月全血细胞计数中出现破碎红细胞,血清乳酸脱氢酶升高,入院前4个月血清肌酐水平缓慢升高,入院前2个月血压显著升高。因此,医生必须意识到TMA是吉西他滨可能的不良事件。就像这个病例一样,接受吉西他滨治疗的患者出现溶血表现和高血压可能有助于早期发现TMA。