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Thoracoscopic retrieval of foreign body after penetrating chest injury: report of two cases. 胸腔镜下胸腔穿透伤后异物取出术附2例报告。
Pub Date : 1999-03-01
Y H Liu, H P Liu, P J Lin, C H Chang

Video-assisted thoracic surgery has proved to be valuable in many settings in thoracic surgery. The use of video-assisted thoracic surgery in trauma has recently rapidly increased. It is useful in acute or delayed management of patients with blunt and penetrating chest trauma. It is safe for removal of clotted hemothorax, treatment of thoracic empyema, treatment of persistent pneumothorax, treatment of chylothorax, and for diagnosis of diaphragmatic injury. We report two cases using thoracoscopy to remove intrathoracic metal fragments and avert the need for thoracotomy. In the first patient, a metal fragment injury was sustained via a penetrating wound from the supraclavicular notch to the right upper lung. The metal fragment was retrieved and the lung was repaired thoracoscopically using conventional suturing techniques. A second patient sustained a broken pin injury to the left upper mediastinum via a low neck wound. The pin was successfully removed under videothoracoscopy. Both patients recovered uneventfully and had shortened hospital stays. We feel that thoracoscopy offers a therapeutic as well as diagnostic benefit in stable patients with penetrating chest trauma.

视频辅助胸外科手术已被证明在许多胸外科手术中是有价值的。视频胸外科手术在创伤中的应用近年来迅速增加。它在钝性和穿透性胸外伤患者的急性或延迟治疗中是有用的。对于清除凝血胸、治疗胸气胸、治疗持续性气胸、治疗乳糜胸以及诊断膈损伤是安全的。我们报告两例使用胸腔镜去除胸内金属碎片,避免了开胸手术的需要。在第一位患者中,金属碎片通过锁骨上切迹到右上肺的穿透伤而受伤。取出金属碎片,并在胸腔镜下使用常规缝合技术修复肺。另一名患者左上纵隔因颈部低位受伤而骨折。胸腔镜下成功取出胸针。两名患者均顺利康复,缩短了住院时间。我们认为胸腔镜在稳定的穿透性胸外伤患者中提供了治疗和诊断的好处。
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引用次数: 0
Dissecting aortic aneurysm complicated with acute disseminated intravascular coagulation: case report. 夹层主动脉瘤并发急性弥散性血管内凝血1例。
Pub Date : 1999-03-01
M C Kuo, P Dunn, P N Wang, H C Shieh, C F Hung

Acute disseminated intravascular coagulation (DIC) is a rare complication of aortic aneurysm with or without dissection. We describe an 88-year-old man who presented with severe hemorrhagic diathesis and a pulsating abdominal mass. An abdominal computed tomography (CT) scan revealed a dissecting abdominal aortic aneurysm with thrombus formation, and his coagulation profile showed the features of acute DIC. After he had received blood component therapy, including fresh frozen plasma and cryoprecipitate concentrates, and intravenous heparin infusion (10,000 U/day), the bleeding diathesis and coagulopathy improved. An aneurysmectomy was performed smoothly without excessive bleeding. Coagulation parameters returned to normal after surgery. Dissecting aortic aneurysm should be considered as a possible etiology of acute disseminated intravascular coagulation, even it occurs in rare situations. Surgical intervention is still the main strategy to normalize coagulopathy. Bleeding diathesis must be corrected before surgery in order to prevent massive intraoperative bleeding.

急性弥散性血管内凝血(DIC)是动脉瘤合并或不合并夹层的罕见并发症。我们描述一个88岁的男子谁提出了严重的出血性素质和脉动腹部肿块。腹部计算机断层扫描(CT)显示夹层腹主动脉瘤伴血栓形成,其凝血特征显示急性DIC特征。患者接受新鲜冷冻血浆、冷沉淀浓缩液等血液成分治疗后,静脉滴注肝素10000 U/d,出血素质及凝血功能改善。动脉瘤切除术顺利进行,无大量出血。术后凝血指标恢复正常。夹层主动脉瘤应被认为是急性弥散性血管内凝血的可能病因,即使它在罕见的情况下发生。手术干预仍是使凝血功能正常化的主要策略。为了防止术中大出血,术前必须纠正出血素质。
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引用次数: 0
Florid osseous dysplasia: case report. 红润骨性发育不良1例。
Pub Date : 1999-03-01
S B Kuo, W H Chen, P C Suen, E C Zen

Florid osseous dysplasia (FOD) is a benign, non-neoplastic lesion characterized by multiple sclerosing masses only within the jawbones. It is most prevalent in middle-aged black women but uncommon in Orientals. Most cases are asymptomatic and should be left untreated. However, the jawbone involved in FOD is very susceptible to infection, including osteomyelitis developed from periodontitis, pulpopathosis, bone biopsy, wearing removable partial dentures, root canal therapy, tooth extraction, inappropriate dental treatment, etc. If secondary osteomyelitis develops, antibiotic and conservative dental therapy treatment is recommended for removing the sources of the odontogenic infection. Surgical removal of inflamed masses is indicated if the inflammatory signs and symptoms are persistent after antibiotic and conservative dental therapy. Here we report a rare FOD case in which an osteomyelitis resulting from generalized periodontitis and bone biopsy was triggered. The patient was accepted for surgery and follow-up in our department. The current literature of this disease is reviewed as well, focusing especially on the clinical manifestations, radiographic features, differential diagnosis, and treatment.

丰润骨性发育不良(FOD)是一种良性非肿瘤性病变,其特征是仅在颌骨内出现多发性硬化肿块。它在中年黑人妇女中最为普遍,但在东方人中并不常见。大多数病例无症状,应不予治疗。然而,患FOD的颌骨非常容易感染,包括牙周炎引起的骨髓炎、牙髓病、骨活检、佩戴可拆卸局部义齿、根管治疗、拔牙、牙科治疗不当等。如果继发性骨髓炎发生,建议使用抗生素和保守的牙科治疗来消除牙源性感染的来源。如果在抗生素和保守的牙科治疗后炎症体征和症状持续存在,则需要手术切除炎性肿块。在此,我们报告一例罕见的FOD病例,该病例由广泛性牙周炎和骨活检引起骨髓炎。患者在我科接受手术及随访。本文也回顾了目前关于本病的文献,特别着重于临床表现、影像学特征、鉴别诊断和治疗。
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引用次数: 0
Cleft of the lip and palate in twins. 双胞胎的唇腭裂。
Pub Date : 1999-03-01
Y C Lin, L J Lo, M S Noordhoff, Y R Chen

Background: Cleft lip and palate is one of the most common congenital anomalies in Taiwan. Its etiology remains unknown for the majority of the patients. The study of twins is a classic method for evaluating the relative roles of genetic and environmental factors in the formation of the anomaly.

Methods: In this study, 37 pairs of twins and one set of triplets with cleft lip and palate were evaluated. Clinical data were collected for zygosity determination and analysis of etiologic factors. The concordance rate and heritability index were assessed.

Results: The results showed that the concordance rate was 26% for all twins and 57% among the monozygotic pairs, which is higher than those rates for the Caucasian population. The heritability index was 53%, higher than the other reports as well. The influence of the environment could not be ruled out.

Conclusion: The results confirm a strong genetic role in the etiology of clefts in our patients. Environmental factors were acting as well. The findings in this study support the multifactorial threshold model in the development of cleft lip and palate.

背景:唇腭裂是台湾最常见的先天性畸形之一。大多数患者的病因尚不清楚。对双胞胎的研究是评估遗传因素和环境因素在异常形成中的相对作用的经典方法。方法:对37对双胞胎和1对三胞胎唇腭裂患者进行评估。收集临床资料进行合子测定和病因分析。评估遗传率和一致性指数。结果:结果显示,所有双胞胎和同卵对的基因一致性率分别为26%和57%,高于高加索人群。遗传力指数为53%,高于其他报道。不能排除环境的影响。结论:本研究结果证实了遗传因素在唇裂发病中的重要作用。环境因素也起了作用。本研究结果支持唇腭裂发育的多因子阈值模型。
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引用次数: 0
Bilateral coronoid process hyperplasia with limitation on mouth opening: case report. 双侧冠突增生伴开口受限1例。
Pub Date : 1999-03-01
W Y Lin, L J Lo, Y R Chen, M S Noordhoff

Coronoid process hyperplasia with limitation of mouth opening is rare. The pathology is often ignored, but it can be easily detected using dental panoramic view of x-ray films. Definition of the coronoid process hyperplasia can be made by measuring the height of coronoid process and the ratio of coronoid/condyle height on lateral cephalometric x-ray film. Etiology of the coronoid process hyperplasia can be congenital or acquired. Differentiation of the diagnosis may be difficult. The congenital type occurs at early age with clinical manifestations. Proposed hypotheses for the formation of coronoid process hyperplasia include increased activity within the temporalis muscle from conditions such as functional stress, compression, and tension. For patients with coronoid process hyperplasia and restriction on mouth opening, conservative treatment should first be attempted. Surgical treatment is considered if conservative treatment fails. Coronoidectomy with early mobilization and aggressive physiotherapy corrects the problem. We present a patient with coronoid process hyperplasia with limitation of mouth opening who was successfully treated.

冠突增生伴开口受限是罕见的。病理常被忽视,但它可以很容易地发现使用牙科全景x线片。通过测量侧位头颅x线片上的冠突高度和冠突/髁突高度之比,可以明确冠突增生的定义。冠突增生的病因可以是先天性的,也可以是后天的。鉴别诊断可能很困难。先天性型发生于早期,有临床表现。冠突增生形成的假设包括由于功能压力、压迫和紧张等条件导致的颞肌活动增加。对于冠突增生及开口受限的患者,应先尝试保守治疗。如果保守治疗失败,可考虑手术治疗。冠状动脉切除术与早期活动和积极的物理治疗纠正了这个问题。我们报告一例冠突增生伴开口受限的患者,并成功治疗。
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引用次数: 0
Timing of shoulder exercise after modified radical mastectomy: a prospective study. 改良乳房根治术后肩部运动时机:一项前瞻性研究。
Pub Date : 1999-03-01
S C Chen, M F Chen

Background: There are several factors those contribute to the amount of axillary drainage after modified radical mastectomy. The drains should be removed as early as possible. Whether the active shoulder movement of the lesion side increases the amount of axillary drainage needs to be studied prospectively.

Methods: From 1994 through 1995, 344 consecutive patients were randomly divided into three groups. One hundred sixteen patients in the early group performed upper arm exercises including pendulum, wall climbing and pulley exercises beginning the third post-operative day. One hundred fifteen patients in the later group patients did the same exercises beginning the sixth post-operative day and 113 patients in the delayed group did the same exercises after all the drains were removed.

Results: There were no significant differences in patient characteristics, including age, body weight, operation methods and the pathology in the three groups. The amount of axilla fossa drainage was significantly less in the patients in the delayed group than in the early and later group (485 ml, 568 ml, 559 ml, respectively, p = 0.032). However, there were no differences in the amount of chest wall site drainage or the number of aspiration of seroma among the three groups. The drains were removed on the average of seventh and ninth post-operative day in the delayed and early group patients, respectively (p = 0.124). Although the range of motion (ROM) of the shoulders in the delayed group patients was slightly limited during the first month after operation, ROM returned at 3 months and no difference was found 6 months after operation.

Conclusion: Upper arm exercise can start after the drains in the axilla are removed. The delay does not limit the shoulder function at 6 months after modified radical mastectomy.

背景:影响改良乳房根治术后腋窝引流量的因素有很多。排水管应尽早清除。病变侧肩部的主动运动是否会增加腋窝引流量,有待于前瞻性研究。方法:1994 ~ 1995年连续344例患者随机分为3组。早期组116例患者从术后第三天开始进行上臂运动,包括摆、爬墙和滑轮运动。115名后发组患者在术后第6天开始做同样的练习,113名后发组患者在所有引流管被移除后也做同样的练习。结果:三组患者的年龄、体重、手术方式、病理等特征均无显著差异。延迟组患者腋窝引流量明显少于早、晚两组(分别为485 ml、568 ml、559 ml, p = 0.032)。三组患者胸壁部位引流量及血肿抽吸次数均无差异。延迟组和早期组患者术后平均第7天、第9天拔除引流管(p = 0.124)。虽然延迟组患者的肩部活动范围(ROM)在术后第一个月略有受限,但在术后3个月时ROM恢复,6个月后无差异。结论:腋窝引流管切除后可进行上臂运动。这种延迟并不限制改良乳房根治术后6个月的肩关节功能。
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引用次数: 0
Pseudomyxoma peritonei with high serum CA19-9: report of three cases. 伴高血清CA19-9的腹膜假性粘液瘤3例报告。
Pub Date : 1999-03-01
C M Kuo, C H Kuo, C S Changchien, K W Chiu, T T Hsu

Pseudomyxoma peritonei (PMP) is an unusual form of intraabdominal neoplasm that produces a large amount of extracellular mucin. It is often associated with mucinous tumors of gastrointestinal tract or ovary. Herein, we report 3 patients with pseudomyxoma peritonei with high serum carbohydrate antigen 19-9 (CA19-9) levels. The first patient, who had a CA19-9 level of 1132 U/ml, had well-differentiated rectal cancer and died of chemotherapy complications, pneumonia and septic shock; one month after admission. The other 2 cases with CA19-9 levels of 2520 U/ml and 679 U/ml had tumors of unknown origins and had survived more than 1 year and 3 months after treatment, respectively. Usually, elevated serum CA19-9 levels are found in patients with pancreatic, biliary, colorectal, gastric or liver cancers. However, many studies have shown high serum CA19-9 levels are associated with mucinous carcinoma. Immunochemical studies also showed positive staining of CA19-9 in mucinous tumors. PMP is composed of large amounts of mucin, therefore, we suggest that serum and ascites CA19-9 levels should be routinely checked in patients with PMP.

腹膜假性黏液瘤(PMP)是一种不寻常的腹内肿瘤,可产生大量的细胞外黏液。常与胃肠道或卵巢黏液性肿瘤有关。本文报告3例血清碳水化合物抗原19-9 (CA19-9)水平较高的腹膜假性黏液瘤患者。1例患者CA19-9水平1132 U/ml,直肠癌高分化,死于化疗并发症、肺炎、感染性休克;入院后一个月。另外2例CA19-9水平分别为2520 U/ml和679 U/ml,肿瘤来源不明,治疗后生存时间分别超过1年和3个月。通常,血清CA19-9水平升高见于胰腺癌、胆道癌、结直肠癌、胃癌或肝癌患者。然而,许多研究表明,高血清CA19-9水平与粘液癌有关。免疫化学研究也显示黏液性肿瘤中CA19-9的阳性染色。PMP由大量粘蛋白组成,因此,我们建议PMP患者应常规检查血清和腹水CA19-9水平。
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引用次数: 0
Hepatocellular carcinoma presenting with acquired porphyria: a case report and review of the literature. 肝细胞癌伴获得性卟啉症:1例报告及文献复习。
Pub Date : 1999-03-01
W S Huang, L Y Liao, C S Wang, P H Chen

Hepatocellular carcinoma (HCC) with acquired porphyria is a very rare condition. It is characterized variably by hyperpigmentation, skin fragility and photodistributed subepidermal vesicles. The serum, urine and/or stool porphyrin levels, usually markedly elevated, can change according to the clinical course. We report here a case of hepatocellular carcinoma presenting with a paraneoplastic syndrome of acquired porphyria. A 73-year-old Chinese woman had the characteristic facial pigmentation of cutaneous porphyria and histologically proven hepatocellular carcinoma. Her serum zinc protoporphyrin was elevated and her urine tested positive for coproporphyrin. Her protoporphyrin and alpha-fetoprotein levels dropped after transarterial chemoembolization treatment. Acquired porphyria in hepatocellular carcinoma occurs exclusively in older persons with huge hepatocellular carcinoma and/or cirrhosis. Before diagnosis, it must be carefully differentiated from inherent porphyrias with HCC, and porphyrias induced by drugs or heavy metal intoxication must be ruled out.

肝细胞癌合并获得性卟啉症是一种非常罕见的疾病。它的不同特征是色素沉着,皮肤脆弱和光分布的表皮下小泡。血清、尿液和/或粪便卟啉水平通常明显升高,可根据临床病程改变。我们在此报告一例肝细胞癌的副肿瘤综合征的获得性卟啉症。一位73岁的中国女性有皮肤卟啉症的特征性面部色素沉着,组织学证实为肝细胞癌。她的血清原卟啉锌升高,她的尿液卟啉检测呈阳性。经动脉化疗栓塞治疗后,原卟啉和甲胎蛋白水平下降。肝细胞癌的获得性卟啉症只发生在患有巨大肝细胞癌和/或肝硬化的老年人中。诊断前必须仔细鉴别与HCC合并的先天性卟啉症,并排除药物或重金属中毒所致的卟啉症。
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引用次数: 0
Comparison of clinical efficacy and adverse effects between extended-release felodipine and slow-release diltiazem in patients with isolated systolic hypertension. 缓释非洛地平与缓释地尔硫卓治疗孤立性收缩期高血压的临床疗效及不良反应比较。
Pub Date : 1999-03-01
M S Chern, F C Lin, D Wu

Background: Isolated systolic hypertension (ISH) is a risk factor for cardiovascular disease. Extended-release felodipine (felodipine ER) has been shown to be effective in the treatment of ISH in Caucasians. However, its pharmacological properties are different from another calcium blocker, diltiazem. Also, the effectiveness, tolerability, and adverse reactions of these two antihypertensive agents for ISH have not been thoroughly assessed in Chinese.

Methods: Sitting blood pressures (BP), heart rate, body weight, adverse reactions, and serum biochemistry were assessed in 70 patients with isolated systolic hypertension (34 treated with felodipine ER and 36 slow-release diltiazem [diltiazem SR] for 10 weeks). Each patient was given 5 mg of felodipine ER or 90 mg of diltiazem SR once daily and was doubled to twice daily if necessary.

Results: Five patients on felodipine ER and four on diltiazem SR withdrew because of intolerable side effects. By ten weeks, 67.6% of the patients responded to a daily dose of 5-10 mg of felodipine ER and 58.3% to a daily dose of 90-180 mg of diltiazem SR. At the end of treatment, felodipine ER lowered the mean BP from 187/83 mmHg at baseline to 149/74 mmHg, whereas diltiazem SR decreased the BP from 185/84 mmHg to 158/78 mmHg (not significant between the two groups). The heart rate did not change significantly in either group. Overall, these two groups of patients had the same rate of adverse reactions (50.0% vs. 50.0%) with similar profiles of the adverse effects.

Conclusion: Equivalent doses of felodipine ER and diltiazem SR are effective first-line monotherapeutic agents for the treatment of ISH.

背景:孤立性收缩期高血压(ISH)是心血管疾病的危险因素。缓释非洛地平(非洛地平ER)已被证明是有效的治疗白种人ISH。然而,它的药理特性与另一种钙阻滞剂地尔硫卓不同。此外,这两种抗高血压药物治疗ISH的有效性、耐受性和不良反应在中国还没有得到充分的评估。方法:观察70例孤立性收缩期高血压患者的坐位血压(BP)、心率、体重、不良反应及血清生化指标(34例给予非洛地平ER治疗,36例给予缓释地尔硫卓[地尔硫卓SR]治疗,疗程10周)。每位患者给予5mg非洛地平ER或90mg地尔硫卓SR每日一次,必要时加倍至每日两次。结果:非洛地平ER组5例,地尔硫卓SR组4例因副作用难以忍受而退出治疗。10周后,67.6%的患者对每日剂量5-10 mg的非洛地平ER有反应,58.3%的患者对每日剂量90-180 mg的地尔硫卓有反应。治疗结束时,非洛地平ER将平均血压从基线时的187/83 mmHg降至149/74 mmHg,而地尔硫卓SR将血压从185/84 mmHg降至158/78 mmHg(两组间无显著差异)。两组的心率都没有明显变化。总体而言,两组患者不良反应发生率相同(50.0% vs 50.0%),不良反应概况相似。结论:等剂量非洛地平ER和地尔硫卓SR是治疗ISH的有效一线单药。
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引用次数: 0
Descending mesocolon defect herniation: case report. 结肠降系膜缺损疝1例。
Pub Date : 1999-03-01
K L Liew, C S Choong, G F Shiau, W C Yang, C M Su

Internal hernia, herniation of the internal organs through defects in the intraabdominal cavity, is rare. Due to the rarity of this pathology and lack of the specific symptoms and signs, early diagnosis and treatment are always stressful to the clinician and misdiagnoses may occur in the emergency room. The prognosis of a patient with uncomplicated internal hernia is excellent. We report a 21-year-old Chinese man with internal herniation through a defect of mesocolon, presented as an impalpable abdominal mass which was shown only on imaging studies. In addition to the typical whirlpool pattern, a huge solid mass between the pancreatic tail and stomach was found under computed tomography (CT) scan. The major symptoms were intermittent epigastralgia and abdominal fullness that had bothered him for years. Physical examination results showed only mild epigastric tenderness. Computed tomography scans and exploratory laparotomy of the abdomen played vital roles during diagnosis. The herniated organ was a portion of jejunum with partial small intestinal obstruction.

腹内疝是一种少见的由腹腔缺损引起的脏器疝。由于这种病理罕见,缺乏特异性的症状和体征,早期诊断和治疗总是给临床医生带来压力,在急诊室可能会出现误诊。无并发症的内疝患者预后良好。我们报告一位21岁的中国男性,因肠系膜缺损而出现腹内疝,表现为难以触及的腹部肿块,仅在影像学检查中表现出来。除了典型的漩涡型外,CT扫描发现胰腺尾部和胃之间有一个巨大的实性肿块。主要症状为间歇性胃脘痛和腹胀,已困扰患者多年。体检结果仅显示轻度上腹压痛。计算机断层扫描和腹部探查术在诊断中起着至关重要的作用。疝出器官为部分空肠伴部分小肠梗阻。
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引用次数: 0
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Changgeng yi xue za zhi
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