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[胰高血糖素瘤综合征中的副肿瘤性痉挛性四肢轻瘫。奥曲肽、达卡巴嗪和α-干扰素治疗成功]

[Paraneoplastic spastic tetraparesis in glucagonoma syndrome. Successful therapy with octreotide, dacarbazine and interferon-alpha].

作者信息

Strohm W D

机构信息

Medizinische Klinik II des Städtischen Krankenhauses Heilbronn, Lehrkrankenhaus der Universität Heidelberg.

出版信息

Z Gastroenterol. 1996 Jul;34(7):438-45.

PMID:8928539
Abstract

Within four years a 44-year-old man developed a glucagonorma syndrome with insulin dependent diabetes mellitus, weight loss, diarrhea, anemia and a marked superinfected eczema. He developed an organo-cerebral psychosyndrome with cognitive retardation and syncoptic disturbance of consciousness, followed by a tetraspasticity with tetraparesis, micturition difficulties and fecal incontinence. There were a general cerebral atrophy as verified by means of MRT and signs of a demyelinating cerebral disease. The plasma concentration of glucagon was 48 fold elevated to 8,536 ng/l. By means of ultrasonography, CT, ERCP, and angiography a tumorous mass of the corpus and tail of the pancreas, 61 x 32 mm in size, was found with signs of infiltration into the region of the aorta and the splenic vein. Furthermore the liver showed diffuse partially cystic metastases. The diagnosis was certified by fine needle biopsy and histologic examination with Grimelius straining. A thrombosis of the femoral vein was detected by CT. The patient was treated by a debulking resection of the corpus and cauda of the pancreas combined with splenectomy and a drug therapy using octreotide. All paraneoplastic symptoms could be widely reduced. Plasma glucagon concentration decreased from 2,200 ng/l to 600 ng/l. Because of a liver enlargement due to the growth of metastases he was successfully treated with dacarbazine 250 mg/m2 per day during six monthly cycles for five days and interferon-alpha 3 x 3 millions units per week for six months followed by a normalization of the liver volumen.

摘要

四年内,一名44岁男性患上了胰高血糖素瘤综合征,伴有胰岛素依赖型糖尿病、体重减轻、腹泻、贫血以及严重的感染性湿疹。他出现了器质性脑精神综合征,伴有认知迟缓以及意识的晕厥性障碍,随后发展为四肢痉挛性四肢轻瘫、排尿困难和大便失禁。磁共振成像(MRT)证实存在一般性脑萎缩以及脱髓鞘性脑病的迹象。胰高血糖素的血浆浓度升高至8536 ng/l,为正常水平的48倍。通过超声检查、CT、内镜逆行胰胆管造影(ERCP)和血管造影,发现胰腺体尾部有一个大小为61×32 mm的肿瘤性肿块,并有浸润至主动脉和脾静脉区域的迹象。此外,肝脏显示有弥漫性部分囊性转移瘤。通过细针穿刺活检和Grimelius染色的组织学检查确诊。CT检测到股静脉血栓形成。患者接受了胰腺体尾部的减瘤切除术,同时进行脾切除术,并使用奥曲肽进行药物治疗。所有副肿瘤症状均得到显著缓解。血浆胰高血糖素浓度从2200 ng/l降至600 ng/l。由于转移瘤生长导致肝脏肿大,他成功接受了达卡巴嗪治疗,每天250 mg/m²,每六周为一个周期,持续五天,同时接受α干扰素治疗,每周3×3百万单位,持续六个月,随后肝脏体积恢复正常。

相似文献

1
[Paraneoplastic spastic tetraparesis in glucagonoma syndrome. Successful therapy with octreotide, dacarbazine and interferon-alpha].[胰高血糖素瘤综合征中的副肿瘤性痉挛性四肢轻瘫。奥曲肽、达卡巴嗪和α-干扰素治疗成功]
Z Gastroenterol. 1996 Jul;34(7):438-45.
2
[Glucagonoma: evolution and treatment].
Rev Med Chil. 2002 Jun;130(6):671-6.
3
Operative and chemotherapeutic management of malignant glucagon-producing tumors.
Surgery. 1981 Oct;90(4):713-9.
4
[Report of a case of glucagonoma misdiagnosed as "eczema" and "hepatic angioma" for three years and review of literature].[一例误诊为“湿疹”和“肝血管瘤”三年的胰高血糖素瘤病例报告及文献复习]
Zhonghua Nei Ke Za Zhi. 1995 Mar;34(3):190-2.
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[Glucagonoma and somatostatinoma].
Nihon Rinsho. 1991 Feb;49 Suppl:672-7.
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Malignant glucagonoma. New options of treatment.恶性胰高血糖素瘤。新的治疗选择。
J Exp Clin Cancer Res. 2006 Mar;25(1):135-9.
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[Malignant glucagonoma: an uncommon cause of new onset diabetes].[恶性胰高血糖素瘤:新发糖尿病的罕见病因]
Endocrinol Nutr. 2011 Apr;58(4):199-201. doi: 10.1016/j.endonu.2010.10.013. Epub 2011 Feb 18.
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[Glucagonoma as a tumor found by the therapist].
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Use of a somatostatin analog (SMS 201-995) in the glucagonoma syndrome.生长抑素类似物(SMS 201-995)在胰高血糖素瘤综合征中的应用。
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[Clinical response of an atypical glucagonoma treated with a long-acting somatostatin analog].[长效生长抑素类似物治疗非典型胰高血糖素瘤的临床反应]
Gastroenterol Clin Biol. 2002 Oct;26(10):926-9.

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