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Interdigitating dendritic cell sarcoma occured alone in axilla. 交叉指状树突状细胞肉瘤单独发生于腋窝。
Pub Date : 2012-05-01 Epub Date: 2012-04-26 DOI: 10.4174/jkss.2012.82.5.330
Sun Wook Han, Zi Sun Kim, Hyuk Moon Kim, Jihyoun Lee, Gil Ho Kang, Hyun Deuk Cho, Sung Yong Kim, Nae Kyeong Park, Cheol Wan Lim, Min Hyk Lee

Interdigitating dendritic cell sarcoma (IDCS) is a very rare disease around the world and its prognosis is known to be aggressive. This reports a case diagnosed as IDCS of the axillary region treated in Soonchunhyang University Hospital. A 57-year-old female visited Soonchunhyang University Hospital with a left axillary mass. The mass was hard and fixed. Computed tomography observed a 7 cm lymph node at the left axilla, and core biopsy suspected sarcoma. In another study, there was no specific finding except the axillary lesion. Left axillary lymph node dissection (level I, II) was conducted and the pathologic report finally showed IDCS. The patient was treated with only radiotherapy and followed up without recurrence for 13 months up to now. IDCS is a very rare sarcoma that is hard to diagnose and progresses fast. Thus, treatment is very difficult. Proper treatment can be better established after more experiences.

间指树突状细胞肉瘤(IDCS)是一种非常罕见的疾病,其预后已知是侵袭性的。本文报告一例在顺天乡大学医院诊断为腋窝区IDCS的病例。一位57岁的女性因左腋窝肿块来到顺天乡大学医院。这团东西又硬又固定。计算机断层扫描发现左侧腋窝有7厘米淋巴结,核心活检怀疑为肉瘤。在另一项研究中,除了腋窝病变外,没有特别的发现。左腋窝淋巴结清扫(ⅰ、ⅱ级),病理报告最终显示IDCS。患者仅行放射治疗,随访13个月,无复发。IDCS是一种非常罕见的肉瘤,难以诊断且进展迅速。因此,治疗非常困难。经过更多的经验,才能更好地建立正确的治疗方法。
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引用次数: 34
Gene expression profiling of papillary thyroid carcinomas in Korean patients by oligonucleotide microarrays. 用寡核苷酸芯片分析韩国患者甲状腺乳头状癌的基因表达谱。
Pub Date : 2012-05-01 Epub Date: 2012-04-26 DOI: 10.4174/jkss.2012.82.5.271
Ki-Wook Chung, Seok Won Kim, Sun Wook Kim

Purpose: The incidence of papillary thyroid carcinomas (PTCs) is rapidly increasing in Korea. Analyzing the gene expression profiling (GEP) of PTCs will facilitate the advent of new methods in diagnosis, prognostication, and treatment. We performed this study to find the GEP of Korean PTCs.

Methods: We performed oligonucleotide microarray analysis with 19 PTCs and 7 normal thyroid glands. Differentially expressed genes were selected using a t-test (|fold| >3) and adjusted Benjamini-Hochberg false discovery rate P-value < 0.01. Quantitative reverse transcription-polymerase chain reaction (QRT-PCR) was used to validate microarray data. A classification model was developed by support vector machine (SVM) algorithm to diagnose PTCs based on molecular signatures.

Results: We identified 79 differentially expressed genes (70 up-regulated and 9 down-regulated) according to the criteria. QRT-PCR for five genes (CDH3, NGEF, PROS1, TGFA, MET) was confirmatory of the microarray data. Hierarchical cluster analysis and a classification model by the SVM algorithm accurately differentiated PTCs from normal thyroid gland based on GEP.

Conclusion: A disease classification model showed excellent accuracy in diagnosing PTCs, thus showing the possibility of molecular diagnosis in the future. This GEP could serve as baseline data for further investigation in the management of PTCs based on molecular signatures.

目的:在韩国,甲状腺乳头状癌(ptc)的发病率正在迅速上升。分析ptc的基因表达谱(GEP)将促进诊断、预后和治疗新方法的出现。我们进行这项研究是为了找出韩国ptc的GEP。方法:对19例ptc和7例正常甲状腺进行寡核苷酸芯片分析。差异表达基因选择采用t检验(|fold| >3),调整benjamin - hochberg错误发现率p值< 0.01。采用定量逆转录聚合酶链反应(QRT-PCR)验证微阵列数据。采用支持向量机(SVM)算法建立了基于分子特征的ptc诊断分类模型。结果:根据标准鉴定出79个差异表达基因(上调70个,下调9个)。5个基因(CDH3, NGEF, PROS1, TGFA, MET)的QRT-PCR验证了微阵列数据。基于GEP的分层聚类分析和支持向量机算法的分类模型能准确区分ptc与正常甲状腺。结论:疾病分类模型对ptc的诊断具有良好的准确性,为分子诊断提供了可能。该GEP可作为基于分子特征的ptc管理进一步研究的基线数据。
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引用次数: 22
Splenectomy affects the balance between hepatic growth factor and transforming growth factor-β and its effect on liver regeneration is dependent on the amount of liver resection in rats. 脾切除术影响大鼠肝脏生长因子和转化生长因子-β之间的平衡,其对肝脏再生的影响与肝切除量有关。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.238
Joohyun Kim, Chang-Ju Kim, Il-Gyu Ko, Sun Hyung Joo, Hyung Joon Ahn

Purpose: Small-for-size syndrome (SFSS) is a major problem in liver surgery, and splenectomy has been used to prevent SFSS. However, it is unknown whether splenectomy has the same effect on liver regeneration in both standard and marginal hepatectomy. The aim of this study is to see a difference in effect of splenectomy on liver regeneration according to the amount of liver resection.

Methods: Thirty male Sprague-Dawley rats (220 to 260 g) were divided into the following five groups: control (n = 6), 70% hepatectomy (n = 6), 70% hepatectomy with splenectomy (n = 6), 90% hepatectomy (n = 6), and 90% hepatectomy with splenectomy (n = 6). The animals were euthanized 24 hours after surgery and liver specimens were obtained. To assess liver regeneration, we performed immunohistochemistry of liver tissue using 5-bromo-2-deoxyuridine (BrdU) labeling and Western blot analysis of hepatic growth factor (HGF) and transforming growth factor-β (TGF-β) in the liver tissue.

Results: The splenectomized subgroup had a higher BrdU-positive cell count in the 90% hepatectomy group, but not in the 70% hepatectomy group (P < 0.001). Splenectomy significantly decreased TGF-β expression (P = 0.005) and increased the HGF to TGF-β ratio (P = 0.002) in the 90% hepatectomy group, but not in the 70% hepatectomy group.

Conclusion: The positive effect of splenectomy on liver regeneration was greater in the group with the larger liver resection. This phenomenon may be related to the relative balance between HGF and TGF-β in the liver.

目的:小体积综合征(SFSS)是肝脏外科手术的主要问题,脾切除术已被用于预防SFSS。然而,脾切除术在标准肝切除术和边缘肝切除术中是否具有相同的肝再生效果尚不清楚。本研究的目的是观察脾切除术对肝再生的影响,根据肝切除量的不同。方法:雄性Sprague-Dawley大鼠30只(220 ~ 260 g),随机分为5组:对照组(n = 6)、70%肝切除组(n = 6)、70%肝切除组(n = 6)、90%肝切除组(n = 6)、90%肝切除组(n = 6)、90%肝切除组(n = 6),术后24 h安乐死,取肝脏标本。为了评估肝再生,我们使用5-溴-2-脱氧尿苷(BrdU)标记对肝组织进行免疫组化,并对肝组织中的肝生长因子(HGF)和转化生长因子-β (TGF-β)进行Western blot分析。结果:脾切除亚组brdu阳性细胞计数高于90%肝切除组,高于70%肝切除组(P < 0.001)。脾切除术显著降低90%肝切除术组TGF-β表达(P = 0.005),提高HGF / TGF-β比值(P = 0.002),而70%肝切除术组无显著差异。结论:脾切除术对肝再生的积极作用在肝切除较大的组更明显。这种现象可能与肝脏中HGF和TGF-β的相对平衡有关。
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引用次数: 18
Oncologic manifestations of neurofibromatosis type 1 in Korea. 韩国1型神经纤维瘤病的肿瘤表现。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.205
Eui Tae Kim, Hwan Namgung, Hyun Deok Shin, Soon Il Lee, Jee Eun Kwon, Myung Chul Chang, Dong Guk Park

Purpose: The aim of this study was to investigate the incidence and spectrum of malignant tumors in Korean neurofibromatosis type 1 (NF1) patients.

Methods: We retrospectively reviewed 125 patients who were diagnosed with NF1 at a single institution from 1995 to 2010. The incidence, location, histologic type, and radiologic findings of malignant tumors as well as development of multiple primary tumors were analyzed.

Results: Eighteen malignant tumors occurred in 16 patients (12.8%) among 125 Korean NF1 patients; 9 carcinomas, 8 sarcomas and 1 central nervous system (CNS) tumor. Five tumors were of nervous system origin and 13 were non-nervous system tumors. The locations of the tumors were as follow: 1 CNS, 2 lung, 3 breast, 3 stomach, 3 small bowel, 1 colon, 1 liver, 1 uterus, 1 neck, and 2 in extremities. Three malignant peripheral nerve sheath tumors (MPNSTs) occurred at the neck and extremity, and one in the liver. All three gastrointestinal stromal tumors (GISTs) had multiple tumors in the jejunum, and one MPNST and one pheochromocytoma were accompanied in two GISTs. Multiple primary tumors, benign or malignant were reported in 4 patients (25.0%), synchronously or metachronously.

Conclusion: Korean NF1 patients had a high risk of developing malignant tumors. The common malignant tumors in Koreans such as breast, lung and stomach cancers developed frequently in addition to the NF1-related tumors such as MPNST or GIST.

目的:探讨韩国1型神经纤维瘤病(NF1)患者恶性肿瘤的发病率和频谱。方法:我们回顾性分析了1995年至2010年在一家机构诊断为NF1的125例患者。分析了恶性肿瘤的发生率、部位、组织学类型、影像学表现及多发原发肿瘤的发展情况。结果:125例韩国NF1患者中发生恶性肿瘤16例,占12.8%;9例癌,8例肉瘤,1例中枢神经系统肿瘤。5例肿瘤来源于神经系统,13例为非神经系统肿瘤。肿瘤发生部位:中枢神经系统1例,肺2例,乳腺3例,胃3例,小肠3例,结肠1例,肝脏1例,子宫1例,颈部1例,四肢2例。三个恶性周围神经鞘肿瘤(MPNSTs)发生在颈部和四肢,一个在肝脏。3例胃肠道间质瘤(gist)均在空肠有多发肿瘤,2例胃肠道间质瘤伴MPNST和嗜铬细胞瘤。多发原发肿瘤,良性或恶性4例(25.0%),同步或异时。结论:韩国NF1患者发生恶性肿瘤的风险较高。除了MPNST、GIST等nf1相关肿瘤外,韩国人常见的乳腺癌、肺癌、胃癌等恶性肿瘤也频繁发生。
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引用次数: 16
A case report of primary breast angiosarcoma with fatal pulmonary hemorrhage due to thrombocytopenia. 原发性乳腺血管肉瘤合并致死性肺出血1例报告。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.251
Yong-Seok Kim, Young-Joong Kim, Kwang-Il Yim, Woo-Chan Park

Primary angiosarcomas of the breast are rare malignancy that account for fewer than 0.04% of all malignant breast tumors. The prognosis is poor. Surgery is the first line of treatment for angiosarcoma. Adjuvant chemotherapy and radiotherapy have been tried, but their efficacy remains controversial. Here we present the case of a 47-year-old woman with a palpable left breast mass that was diagnosed as a primary angiosarcoma. The patient underwent modified radical mastectomy with adjuvant chemotherapy and radiotherapy. Postoperatively, eighteen months later, the angiosarcoma recurred. The patient returned complaining of dyspnea and hemoptysis and was found to have a large pleural effusion. She developed a gradual onset of thrombocytopenia that persisted despite platelet transfusions. Finally, the patient died of respiratory failure secondary to pulmonary hemorrhage.

乳腺原发性血管肉瘤是一种罕见的恶性肿瘤,占乳腺恶性肿瘤的不到0.04%。预后很差。手术是治疗血管肉瘤的第一道防线。辅助化疗和放疗已经尝试过,但其疗效仍存在争议。我们在此报告一位47岁女性,左乳房肿块可触及,诊断为原发性血管肉瘤。患者行改良根治性乳房切除术并辅以化疗和放疗。术后18个月,血管肉瘤复发。病人回来后主诉呼吸困难和咯血,并发现有大量胸腔积液。她逐渐出现血小板减少症,尽管输了血小板,但仍持续存在。最后,患者死于肺出血继发的呼吸衰竭。
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引用次数: 5
Adrenocortical tumors in children 18 years old and younger. 18岁及以下儿童的肾上腺皮质肿瘤。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.246
Min Jeng Cho, Dae Yeon Kim, Seong Chul Kim, Tae Hoon Kim, In Koo Kim

Purpose: Pediatric adrenocortical tumors (ACTs) are rare. We reviewed findings in 8 children, 18 years of age or younger, diagnosed with ACT in our institution over the past 15 years.

Methods: We retrospectively reviewed 8 children with ACTs treated between 1996 and 2010.

Results: Three girls and 5 boys were treated for ACTs; their median age at presentation was 144 months (range, 28 months to 18 years). Seven patients showed signs of endocrine dysfunction, 4 with Cushing syndrome, 2 with virilization, and 1 with hyperaldosteronism. One patient, with symptoms of hematuria, underwent a computed tomography scan, which showed an adrenal mass. The median duration of symptoms prior to resection was 6 months (range, 1 to 24 months). Five patients had adenomas and 3 had carcinomas. All underwent complete resection of the tumor, with laparoscopic adrenalectomy performed on 3 patients with adenoma and 1 with carcinoma. The median tumor weight was 12.5 g (range, 1 to 130 g) and the median tumor volume was 18.3 cm(3) (range, 2.2 to 299.2 cm(3)). At a median follow-up of 5.1 years (range, 4 months to 15 years), all 8 patients remain alive with no recurrence of disease.

Conclusion: The characteristics of pediatric ACTs vary considerably. Laboratory findings, clinical hormonal features, and tumor size could not distinguish adenomas from carcinomas before surgery. Complete tumor resection was successful, with no tumor recurrence. However, the small number of patients and short follow-up period limit assessments of prognosis.

目的:小儿肾上腺皮质肿瘤是一种罕见的肿瘤。我们回顾了过去15年来在我们机构诊断为ACT的8名儿童,年龄在18岁或以下。方法:回顾性分析1996年至2010年间8例接受ACTs治疗的患儿。结果:3名女孩和5名男孩接受ACTs治疗;患者就诊时的中位年龄为144个月(范围28个月至18岁)。内分泌功能障碍7例,库欣综合征4例,男性化2例,高醛固酮增多症1例。一名有血尿症状的患者接受了计算机断层扫描,显示肾上腺肿块。切除前症状的中位持续时间为6个月(范围为1至24个月)。5例有腺瘤,3例有癌。所有患者均行肿瘤全切除术,其中3例腺瘤患者行腹腔镜肾上腺切除术,1例癌患者行腹腔镜肾上腺切除术。中位肿瘤重量12.5 g(范围1 ~ 130 g),中位肿瘤体积18.3 cm(范围2.2 ~ 299.2 cm(3))。中位随访5.1年(4个月至15年),所有8例患者均存活,无疾病复发。结论:儿童ACTs的特点差异很大。术前实验室检查、临床激素特征和肿瘤大小不能区分腺瘤和癌。肿瘤完全切除成功,无复发。然而,患者数量少,随访时间短,限制了对预后的评估。
{"title":"Adrenocortical tumors in children 18 years old and younger.","authors":"Min Jeng Cho,&nbsp;Dae Yeon Kim,&nbsp;Seong Chul Kim,&nbsp;Tae Hoon Kim,&nbsp;In Koo Kim","doi":"10.4174/jkss.2012.82.4.246","DOIUrl":"https://doi.org/10.4174/jkss.2012.82.4.246","url":null,"abstract":"<p><strong>Purpose: </strong>Pediatric adrenocortical tumors (ACTs) are rare. We reviewed findings in 8 children, 18 years of age or younger, diagnosed with ACT in our institution over the past 15 years.</p><p><strong>Methods: </strong>We retrospectively reviewed 8 children with ACTs treated between 1996 and 2010.</p><p><strong>Results: </strong>Three girls and 5 boys were treated for ACTs; their median age at presentation was 144 months (range, 28 months to 18 years). Seven patients showed signs of endocrine dysfunction, 4 with Cushing syndrome, 2 with virilization, and 1 with hyperaldosteronism. One patient, with symptoms of hematuria, underwent a computed tomography scan, which showed an adrenal mass. The median duration of symptoms prior to resection was 6 months (range, 1 to 24 months). Five patients had adenomas and 3 had carcinomas. All underwent complete resection of the tumor, with laparoscopic adrenalectomy performed on 3 patients with adenoma and 1 with carcinoma. The median tumor weight was 12.5 g (range, 1 to 130 g) and the median tumor volume was 18.3 cm(3) (range, 2.2 to 299.2 cm(3)). At a median follow-up of 5.1 years (range, 4 months to 15 years), all 8 patients remain alive with no recurrence of disease.</p><p><strong>Conclusion: </strong>The characteristics of pediatric ACTs vary considerably. Laboratory findings, clinical hormonal features, and tumor size could not distinguish adenomas from carcinomas before surgery. Complete tumor resection was successful, with no tumor recurrence. However, the small number of patients and short follow-up period limit assessments of prognosis.</p>","PeriodicalId":49157,"journal":{"name":"Journal of the Korean Surgical Society","volume":"82 4","pages":"246-50"},"PeriodicalIF":0.0,"publicationDate":"2012-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4174/jkss.2012.82.4.246","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30566995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Primary tuberculosis appendicitis with mesenteric mass. 原发性结核性阑尾炎伴肠系膜肿块。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.266
So-Hyun Nam, Jin Soo Kim, Ki Hoon Kim, Sung Jin Park

Tuberculosis primarily affecting the appendix is extremely rare and the diagnosis is difficult. Here, we report the case of a 14-year-old healthy boy presenting with right lower quadrant abdominal pain. On computed tomography, the distended appendix with 3.3 × 2.7 cm mass located at the right side of the right iliac artery was detected. There was neither bowel wall thickening nor active lung lesion. After laparoscopic appendectomy with mass excision, histopathological examination revealed chronic granulomatous inflammation, with caseous necrosis of the appendix. We made a diagnosis of primary tuberculosis of appendix and administrated anti-tuberculosis medication.

主要影响阑尾的结核病极为罕见,诊断困难。在这里,我们报告一个14岁的健康男孩的情况下表现为右下腹部疼痛。ct示阑尾扩张,肿物3.3 × 2.7 cm,位于右髂动脉右侧。无肠壁增厚,无活动性肺病变。腹腔镜阑尾切除术并肿块切除后,组织病理学检查显示慢性肉芽肿性炎症,伴阑尾干酪样坏死。我们诊断为原发性阑尾结核并给予抗结核药物治疗。
{"title":"Primary tuberculosis appendicitis with mesenteric mass.","authors":"So-Hyun Nam,&nbsp;Jin Soo Kim,&nbsp;Ki Hoon Kim,&nbsp;Sung Jin Park","doi":"10.4174/jkss.2012.82.4.266","DOIUrl":"https://doi.org/10.4174/jkss.2012.82.4.266","url":null,"abstract":"<p><p>Tuberculosis primarily affecting the appendix is extremely rare and the diagnosis is difficult. Here, we report the case of a 14-year-old healthy boy presenting with right lower quadrant abdominal pain. On computed tomography, the distended appendix with 3.3 × 2.7 cm mass located at the right side of the right iliac artery was detected. There was neither bowel wall thickening nor active lung lesion. After laparoscopic appendectomy with mass excision, histopathological examination revealed chronic granulomatous inflammation, with caseous necrosis of the appendix. We made a diagnosis of primary tuberculosis of appendix and administrated anti-tuberculosis medication.</p>","PeriodicalId":49157,"journal":{"name":"Journal of the Korean Surgical Society","volume":"82 4","pages":"266-9"},"PeriodicalIF":0.0,"publicationDate":"2012-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4174/jkss.2012.82.4.266","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30566999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Laparoscopic reversal of Hartmann's procedure. 哈特曼手术的腹腔镜逆转。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.256
Joong-Min Park, Kyong-Choun Chi

Reversal of Hartmann's procedure is a major surgical procedure associated with significant morbidity and mortality. Because of the difficulty of the procedure, laparoscopic reversal of Hartmann's procedure is not well established. We describe our experience with this laparoscopic procedure to assess its difficulty and safety. Five patients (4 men and 1 woman) underwent laparoscopic reversal of Hartmann's procedure (LRHP). The initial surgeries were performed to manage obstructive colorectal cancer for 4 patients, and rectovesical fistula for one patient. The procedure was laparoscopically completed for 4 patients. Conversion to open laparotomy was required for one patient, secondary to massive adhesion in lower abdomen. Transient ileostomies were made in 2 cases. Operative time ranged from 240 to 545 minutes. There was no operative mortality. LRHP can be performed safely by an experienced surgeon. However, it is still technically challenging and time consuming.

哈特曼手术逆转是一种主要的外科手术,与显著的发病率和死亡率相关。由于手术的难度,腹腔镜下哈特曼手术的逆转尚未得到很好的建立。我们描述我们的经验与腹腔镜手术评估其难度和安全性。5例患者(4男1女)行腹腔镜哈特曼手术逆转(LRHP)。4例为梗阻性结直肠癌,1例为直肠膀胱瘘。4例患者在腹腔镜下完成手术。1例患者继发于下腹大量粘连,需转开腹手术。暂时性回肠造口2例。手术时间240 ~ 545分钟。无手术死亡率。LRHP可以由经验丰富的外科医生安全地进行。然而,它在技术上仍然具有挑战性和耗时。
{"title":"Laparoscopic reversal of Hartmann's procedure.","authors":"Joong-Min Park,&nbsp;Kyong-Choun Chi","doi":"10.4174/jkss.2012.82.4.256","DOIUrl":"https://doi.org/10.4174/jkss.2012.82.4.256","url":null,"abstract":"<p><p>Reversal of Hartmann's procedure is a major surgical procedure associated with significant morbidity and mortality. Because of the difficulty of the procedure, laparoscopic reversal of Hartmann's procedure is not well established. We describe our experience with this laparoscopic procedure to assess its difficulty and safety. Five patients (4 men and 1 woman) underwent laparoscopic reversal of Hartmann's procedure (LRHP). The initial surgeries were performed to manage obstructive colorectal cancer for 4 patients, and rectovesical fistula for one patient. The procedure was laparoscopically completed for 4 patients. Conversion to open laparotomy was required for one patient, secondary to massive adhesion in lower abdomen. Transient ileostomies were made in 2 cases. Operative time ranged from 240 to 545 minutes. There was no operative mortality. LRHP can be performed safely by an experienced surgeon. However, it is still technically challenging and time consuming.</p>","PeriodicalId":49157,"journal":{"name":"Journal of the Korean Surgical Society","volume":"82 4","pages":"256-60"},"PeriodicalIF":0.0,"publicationDate":"2012-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4174/jkss.2012.82.4.256","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30566997","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 24
Impact of chronologic age in the elderly with gastric cancer. 年龄对老年胃癌患者的影响。
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.211
Sung Ryol Lee, Hyung Ook Kim, Chang Hak Yoo

Purpose: Although the incidence of gastric cancer has declined in the general population, it is the second most frequent cause of death due to malignancy in the world with its incidence in the elderly increasing as a result of increased life expectancy. This present study tried to find the optimal treatment for patients aged 75 years or older with gastric cancer through comparison of the clinicopathological characteristics, surgical outcomes, and identifying prognostic factors of survival.

Methods: Elderly patients who underwent gastric resection for gastric cancer from January, 1999 to February, 2009 (n = 470) were divided into two groups: very elderly patients, 75 years or older (n = 95), and younger elderly patients, between 65 and 74 years old (n = 365).

Results: Distinct characteristics of very elderly patients included more frequent underlying disease, deeper invasion, and more frequent lymph node metastasis. There were significant differences in overall survival between the two groups at stages III-B and IV. However, postoperative hospital stays, postoperative morbidity, mortality and early stage did not differ between curatively resected patients in the two groups.

Conclusion: Due to improved postoperative care, gastrectomy of gastric cancer is the treatment of choice in very elderly patients. Therefore, early diagnosis through regular medical screening and curative gastrectomy with lymph node dissection should be performed in very elderly gastric cancer patients.

目的:虽然胃癌在一般人群中的发病率有所下降,但它是世界上第二大恶性肿瘤导致死亡的原因,随着预期寿命的延长,老年人的发病率也在增加。本研究旨在通过比较75岁及以上高龄胃癌患者的临床病理特征、手术结果以及确定影响生存的预后因素,寻找最佳的治疗方案。方法:选取1999年1月~ 2009年2月行胃癌切除术的老年患者470例(n = 470),分为75岁以上高龄患者95例和65 ~ 74岁较年轻老年患者365例。结果:高龄患者的明显特征包括更频繁的基础疾病、更深的侵袭和更频繁的淋巴结转移。两组患者在III-B期和IV期的总生存率有显著差异。然而,两组患者的术后住院时间、术后发病率、死亡率和早期生存率没有差异。结论:由于术后护理水平的提高,胃切除术是高龄胃癌患者的首选治疗方法。因此,高龄胃癌患者应通过定期医学筛查进行早期诊断,并行根治性胃切除术并淋巴结清扫。
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引用次数: 19
Postoperative pneumoperitoneum: guilty or not guilty? 术后气腹:有罪还是无罪?
Pub Date : 2012-04-01 Epub Date: 2012-03-27 DOI: 10.4174/jkss.2012.82.4.227
Chang Ho Lee, Jong Hun Kim, Min Ro Lee

Purpose: The aim of this study was to determine the incidence and duration of postoperative pneumoperitoneum on plain radiographs and to identify the radiologic findings associated with anastomotic leakage.

Methods: A retrospective analysis was conducted on plain radiographs of 384 patients who underwent intra-abdominal anastomoses between March 2005 and December 2008.

Results: Of the 384 patients, 93 patients (24.2%) had postoperative pneumoperitoneums. Of the 93 patients, 86 patients (92.5%) had physiologic pneumoperitoneums and 7 patients (7.5%) had pneumoperitoneums associated with anastomotic leakage. The initial air height was significantly greater in the leakage group than the physiologic air group (12.16 ± 7.65 mm vs. 7.71 ± 5.08 mm, P = 0.04). The area under the receiver operating characteristic curve of the initial height of free air for anastomotic leakage was 0.69 (95% confidence interval, 0.59 to 0.78). The best cut-off point was 11.7 mm. The height of the pneumoperitoneum increased with time in the leakage group. Ileus was significantly more prevalent in the leakage group than the physiologic air group (P < 0.01).

Conclusion: Postoperative pneumoperitoneum is a common phenomenon after abdominal surgery. An initial air height >11.7 mm, increasing air height over time, and the presence of ileus on plain radiographs suggest a high likelihood of anastomotic leakage.

目的:本研究的目的是在x线平片上确定术后气腹的发生率和持续时间,并确定与吻合口瘘相关的放射学表现。方法:回顾性分析2005年3月至2008年12月行腹腔吻合术的384例患者的x线平片资料。结果:384例患者中,术后发生气腹93例(24.2%)。93例患者中,生理性气腹86例(92.5%),吻合口漏气腹7例(7.5%)。漏气组的初始空气高度明显高于生理空气组(12.16±7.65 mm vs. 7.71±5.08 mm, P = 0.04)。吻合口漏自由空气初始高度受术者工作特征曲线下面积为0.69(95%可信区间0.59 ~ 0.78)。最佳分界点为11.7 mm。渗漏组气腹高度随时间增加。漏气组肠梗阻发生率明显高于生理气组(P < 0.01)。结论:术后气腹是腹部手术后常见的现象。初始空气高度>11.7 mm,随着时间的推移空气高度增加,x平片上出现肠梗阻,提示吻合口瘘的可能性很大。
{"title":"Postoperative pneumoperitoneum: guilty or not guilty?","authors":"Chang Ho Lee,&nbsp;Jong Hun Kim,&nbsp;Min Ro Lee","doi":"10.4174/jkss.2012.82.4.227","DOIUrl":"https://doi.org/10.4174/jkss.2012.82.4.227","url":null,"abstract":"<p><strong>Purpose: </strong>The aim of this study was to determine the incidence and duration of postoperative pneumoperitoneum on plain radiographs and to identify the radiologic findings associated with anastomotic leakage.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on plain radiographs of 384 patients who underwent intra-abdominal anastomoses between March 2005 and December 2008.</p><p><strong>Results: </strong>Of the 384 patients, 93 patients (24.2%) had postoperative pneumoperitoneums. Of the 93 patients, 86 patients (92.5%) had physiologic pneumoperitoneums and 7 patients (7.5%) had pneumoperitoneums associated with anastomotic leakage. The initial air height was significantly greater in the leakage group than the physiologic air group (12.16 ± 7.65 mm vs. 7.71 ± 5.08 mm, P = 0.04). The area under the receiver operating characteristic curve of the initial height of free air for anastomotic leakage was 0.69 (95% confidence interval, 0.59 to 0.78). The best cut-off point was 11.7 mm. The height of the pneumoperitoneum increased with time in the leakage group. Ileus was significantly more prevalent in the leakage group than the physiologic air group (P < 0.01).</p><p><strong>Conclusion: </strong>Postoperative pneumoperitoneum is a common phenomenon after abdominal surgery. An initial air height >11.7 mm, increasing air height over time, and the presence of ileus on plain radiographs suggest a high likelihood of anastomotic leakage.</p>","PeriodicalId":49157,"journal":{"name":"Journal of the Korean Surgical Society","volume":"82 4","pages":"227-31"},"PeriodicalIF":0.0,"publicationDate":"2012-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4174/jkss.2012.82.4.227","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30567578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
期刊
Journal of the Korean Surgical Society
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