Tonsillectomy in a patient with hereditary angioedema after prophylaxis with C1 inhibitor concentrate.

Annals of allergy Pub Date : 1994-11-01
K K Maves, J M Weiler
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Abstract

Background: A 15-year-old young man with a history of recurrent streptococcal pharyngitis and hereditary angioedema presented for tonsillectomy. Preoperative physical examination was normal with the exception of enlarged pharyngeal tonsils with crypts and pustules; there was no evidence of angioedema. Laboratory studies were remarkable for a C4 level of 8 mg/dL (normal 20-50 mg/dL) and C1 inhibitor (C1 INH) level of 4 mg/dL (normal 11-26 mg/dL).

Objective: To report the use of C1 INH concentrate as prophylactic treatment for a patient with hereditary angioedema who required tonsillectomy.

Methods: The patient was treated with stanozolol 4 mg po quid and clindamycin 150 mg po tid during the week before the procedure. Two hours prior to surgery, he received 2300 plasma units of intravenous C1-inhibitor (Human) Vapor Heated, IMMUNO (IMMUNO Clinical Research Corporation, New York, NY).

Results: Approximately eight hours after an uncomplicated tonsillectomy, the patient began to experience crampy abdominal pain, typical of his hereditary angioedema. Beginning 22 hours after surgery, he had facial swelling and complained of difficulty swallowing and the sensation of throat swelling. The symptoms resolved over the next eight hours. Serial laboratory examinations revealed: [table: see text]

Conclusions: We believe that the occurrence of abdominal pain, facial swelling, and difficulty swallowing suggests that this patient may have experienced a mild, generalized flare of hereditary angioedema during the postoperative period in spite of prophylactic therapy with both anabolic steroids and C1 INH concentrate. This serves as a reminder that patients with hereditary angioedema require close observation following invasive procedures even after premedication with stanozolol and C1 INH concentrate.

C1抑制剂浓缩预防后遗传性血管性水肿患者的扁桃体切除术。
背景:一名15岁的年轻人,有复发性链球菌性咽炎和遗传性血管性水肿的病史,提出扁桃体切除术。术前体格检查除咽扁桃体肿大伴隐窝及脓疱外,其余正常;没有血管水肿的迹象。实验室研究显示C4水平为8 mg/dL(正常20-50 mg/dL), C1抑制剂(C1 INH)水平为4 mg/dL(正常11-26 mg/dL)。目的:报道1例遗传性血管性水肿需要扁桃体切除术的患者使用C1 INH浓缩液进行预防性治疗。方法:术前1周给予司他唑尔4 mg /次,克林霉素150 mg /次。手术前两小时,他接受了2300血浆单位的静脉注射c1抑制剂(人)蒸汽加热,IMMUNO (IMMUNO临床研究公司,纽约,NY)。结果:无并发症扁桃体切除术后约8小时,患者开始出现痉挛性腹痛,典型的遗传性血管性水肿。术后22小时开始,患者出现面部肿胀、吞咽困难、咽喉肿胀感。在接下来的8个小时里症状消失了。结论:我们认为,腹痛、面部肿胀和吞咽困难的出现表明,尽管使用了合成代谢类固醇和C1 INH浓缩物进行预防性治疗,但该患者可能在术后期间经历了轻度、全身性遗传性血管性水肿发作。这提醒我们,遗传性血管性水肿患者需要在侵入性手术后进行密切观察,即使在用药前使用斯坦诺唑尔和C1 INH浓缩物。
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