Successful laparoscopic extirpation of a vasoactive intestinal polypeptide‐secreting neuroblastoma originating from the right adrenal gland: A report of an infantile case

Successful laparoscopic extirpation of a vasoactive intestinal polypeptide‐secreting neuroblastoma originating from the right adrenal gland: A report of an infantile case
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成功腹腔镜摘除源自右肾上腺的血管活性肠多肽分泌神经母细胞瘤:一例婴儿病例报告

DOI:
10.1111/ases.12916
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发表时间:
2021
影响因子:
1
通讯作者:
Ieiri Satoshi
Ieiri Satoshi
中科院分区:
--
文献类型:
--
作者:
Sugita Koshiro;Kaji Tatsuru;Muto Mitsuru;Nishikawa Takuro;Okamoto Yasuhiro;Imamura Mari;Ieiri Satoshi

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我们在此报告一名10个月大的女婴,有4个月的腹泻史,伴电解质异常和生长障碍。计算机断层扫描检测到一个4 cm右肾上腺肿瘤。在肿瘤中,I123-间碘苄胍放射性造影未发现转移或蓄积。疑似血管活性肠肽分泌性神经母细胞瘤,开始奥曲肽治疗,但腹泻持续。在腹腔镜下进行肿瘤摘除术。肿瘤切除后,症状立即改善,她的生长在手术后9个月赶上。小儿实体瘤的微创治疗是困难的,特别是神经母细胞瘤,但可能有利于患者的恢复。
We herein report a 10‐month‐old female infant with a 4‐month history of diarrhea with electrolyte abnormalities and growth impairment. A 4‐cm right adrenal tumor was detected by computed tomography. No metastasis or accumulation on I123‐metaiodobenzylguanidine scintigraphy was recognized in the tumor. A vasoactive intestinal peptide‐secreting neuroblastic tumor was suspected, and octreotide was started, but the diarrhea persisted. Tumor extirpation was laparoscopically performed. After tumor removal, the symptoms improved immediately, and her growth caught up by 9 months after surgery. A minimally invasive approach for pediatric solid tumor is difficult, especially for neuroblastoma, but may be beneficial for the patient's recovery.
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发表时间: 2007-12-01
影响因子: 3.2
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