1.Gastric Duplication Cyst Removed by Endoscopic Submucosal Dissection.
Jung Seop EOM ; Gwang Ha KIM ; Geun Am SONG ; Dong Hoon BAEK ; Kwang Duck RYU ; Kyung Nam LEE ; Do Youn PARK
The Korean Journal of Gastroenterology 2011;58(6):346-349
Duplication cysts are uncommon congenital malformations that may occur anywhere throughout the alimentary tract. The stomach is an extremely rare site of occurrence. Here, we report a case of gastric duplication cyst initially presenting with a gastric submucosal tumor. A 28-year-old man complained of dyspepsia lasting 1 year and upper endoscopy revealed an ellipsoid submucosal tumor at the greater curvature of the antrum. We intended to use the injection-and-cut technique: however, after saline injection, the lesion was dented and impossible to grasp with a snare. Therefore, we decided to perform endoscopic submucosal dissection and removed the tumor without complication. Histopathology revealed a 0.6x0.6 cm-sized duplication cyst, and there has been no recurrence in 2 years.
Adult
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Cysts/congenital/*pathology/*surgery
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Dissection
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Gastric Mucosa/*pathology/*surgery
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*Gastroscopy
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Humans
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Male
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Pyloric Antrum/pathology
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Stomach Diseases/*pathology/*surgery/ultrasonography
2.Plexiform Angiomyxoid Myofibroblastic Tumor of the Stomach: A Case Report.
Aeri KIM ; Young Kyung BAE ; Hyeong Chan SHIN ; Joon Hyuk CHOI
Journal of Korean Medical Science 2011;26(11):1508-1511
Plexiform angiomyxoid myofibroblastic tumor (PAMT) is a recently described mesenchymal tumor of the stomach. We report the first case of PAMT in Korea. A 52-yr-old man underwent esophagogastroduodenoscopy due to dyspepsia for 2 yr. There was a submucosal mass with small mucosal ulceration in the gastric antrum. The tumor measured 3.5 x 2.3 cm in size and showed multinodular plexiform growth pattern of bland-looking spindle cells separated by an abundant myxoid or fibromyxoid matrix rich in small thin-walled blood vessels. The tumor cells were negative for CD117 (c-KIT), CD34 and S-100 protein, but diffusely positive for smooth muscle actin consistent with predominant myofibroblastic differentiation. The patient is doing well without recurrence or metastasis for 5 months after surgery. Although there have been limited follow-up data, PAMT is regarded as a benign gastric neoplasm with histological and immunohistochemical charateristics distinguished from gastrointestinal stromal tumor and other mesenchymal tumors of the stomach.
Dyspepsia/diagnosis
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Endoscopy, Digestive System
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Humans
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Male
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Middle Aged
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Myofibroblasts
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*Myxoma/diagnosis/pathology/surgery
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Pyloric Antrum/pathology
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*Stomach Neoplasms/diagnosis/pathology/surgery
3.Torus Hyperplasia of the Pyloric Antrum.
Chi Hun KIM ; Hye Seung HAN ; Sun Young LEE ; Byung Kook KIM ; In Kyung SUNG ; Moo Kyung SEONG ; Kyung Yung LEE
Journal of Korean Medical Science 2010;25(1):152-154
Primary or idiopathic hypertrophy of the pyloric muscle in adult, so called torus hyperplasia, is an infrequent but an established entity. It is caused by a circular muscle hypertrophy affecting the lesser curvature near the pylorus. Since most of the lesions are difficult to differentiate from tumor, distal gastrectomy is usually preformed to rule out most causes of pyloric lesions including neoplastic ones through a pathological study. A 56-yr-old man with a family history of gastric cancer presented with abdominal discomfort of 1 month duration. Upper gastrointestinal endoscopy showed a 1.0 cm sized irregular submucosal lesion proximal to the pylorus to the distal antrum on the lesser curvature. On colonoscopy examination, a 1.5 cm sized protruding mass was noticed on the appendiceal orifice. Gastrectomy and cecectomy were done, and histological section revealed marked hypertrophy of the distal circular pyloric musculature and an appendiceal mucocele. To the best of our knowledge, this is the first case of torus hyperplasia with appendiceal mucocele which is found incidentally.
Cystadenoma, Mucinous/diagnosis
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Endoscopy, Gastrointestinal
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Gastrectomy
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Humans
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Hyperplasia/diagnosis/pathology/surgery
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Male
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Middle Aged
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Pyloric Antrum/*pathology/surgery
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Tomography, X-Ray Computed
4.Comparison of clinicopathological features and prognosis between adenocarcinoma of esophagogastric junction and adenocarcinoma of gastric antrum.
Ziyu ZHU ; Yimin WANG ; Fengke LI ; Jialiang GAO ; Bangling HAN ; Rui WANG ; Yingwei XUE
Chinese Journal of Gastrointestinal Surgery 2019;22(2):149-155
OBJECTIVE:
To compare the clinicopathological features and the prognosis between patients with adenocarcinoma of esophagogastric junction (AEG) and with adenocarcinoma of gastric antrum (AGA), and to investigate the prognostic factors of AEG and AGA.
METHODS:
A retrospective cohort study was performed on clinicopathological data of 239 AEG patients (AEG group) and 313 AGA patients selected simultaneously (AGA group) undergoing operation at Harbin Medical University Cancer Hospital from January 2001 to December 2012.
INCLUSION CRITERIA:
(1) receiving radical surgery (R0 resection); (2) AEG or AGA confirmed by pathological examination of postoperative tissue specimens; (3) without preoperative neoadjuvant radiotherapy or chemotherapy; (4) complete clinicopathological and follow-up data; (5) patients who died of non-tumor-related causes were excluded. Chi-square test and independent samples t-test were used to determine differences in clinicopathological factors between two groups. The overall survival (OS) of patients was compared by Kaplan-Meier method and Log-rank test. Multivariate prognosis analysis was performed using Cox proportional hazards regression model.
RESULTS:
As compared to AGA group, AEG group had higher proportion of male [82.0%(196/239) vs. 65.2%(204/313),χ²=19.243,P<0.001], older age [(60±10) years vs. (55±12) years, t=4.895, P<0.001], larger tumor diameter [(5.6±2.4) cm vs. (5.0±3.3) cm, t=2.480,P=0.013], more T4 stage[64.8%(155/239) vs. 55.6%(174/313),Z=-3.998, P<0.001], and more advanced tumor stage [stage III:60.7%(145/239) vs. 55.6%(174/313),Z=-2.564,P=0.010]. There were no statistically significant differences in serum albumin or hemoglobin between two groups (all P>0.05). The 5-year OS rate was 33.5% and 56.9% in AEG group and AGA group respectively and the median OS was 60.0(3.0-60.0) months and 33.6(3.0-60.0) months respectively; the difference was statistically significant (P<0.001). In AEG group, univariate analysis showed that differences of hemoglobin level (5-year OS rate: 24.0% for <130 g/L, 39.9% for ≥130 g/L, P=0.006), tumor diameter (5-year OS rate: 41.9% for <5 cm,28.8% for ≥5 cm, P=0.014), N stage (5-year OS rate: 42.2% for N0, 40.9% for N1, 31.7% for N2, 15.8% for N3a, 9.0% for N3b, P<0.001) and TNM stage (5-year OS rate: 56.2% for stage I, 38.5% for stage II, 28.3% for stage III,P=0.017) were statistically significant (all P<0.05); multivariate analysis revealed that the worse N stage was an independent risk factor of prognosis survival for AEG patients(HR=1.404,95%CI:1.164-1.693, P<0.001), and serum hemoglobin level ≥130 g/L was an independent protective factor of prognosis survival for AEG patients (HR=0.689,95%CI:0.501-0.946,P=0.021). In AGA group, univariate analysis showed that differences of serum albumin (5-year OS rate: 49.1% for <40 g/L, 61.1% for ≥ 40 g/L, P=0.021), tumor diameter (5-year OS rate: 74.2% for <5 cm, 39.9% for ≥ 5 cm, P<0.001), T stage (5-year OS rate: 98.3% for T1,83.3% for T2,50.0% for T3,36.8% for T4, P<0.001), N stage (5-year OS rate: 89.0% for N0, 62.3% for N1, 50.0% for N2, 33.9% for N3a, 10.3% for N3b, P<0.001) and TNM stage (5-year OS rate: 97.3% for stage I, 75.8% for stage II, 32.8% for stage III, P<0.001) were statistically significant (all P<0.05); multivariate analysis revealed that the worse T stage (HR=1.516,95%CI:1.060-2.167,P=0.023) and the worse N stage (HR=1.453,95%CI:1.209-1.747,P<0.001) were independent risk factors for prognosis of AGA patients.
CONCLUSIONS
As compared to AGA, AEG presents have poorer prognosis,and is easier to present with later pathological stage and larger tumor diameter. N stage and hemoglobin level are independent factors associated with the OS of AEG patients. T stage and N stage are independent factors associated with the OS of AGA patients.
Adenocarcinoma
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mortality
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pathology
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surgery
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Adult
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Aged
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Esophagogastric Junction
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pathology
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surgery
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Female
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Humans
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Kaplan-Meier Estimate
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Male
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Middle Aged
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Neoplasm Staging
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Prognosis
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Pyloric Antrum
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pathology
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surgery
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Retrospective Studies
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Stomach Neoplasms
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mortality
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pathology
;
surgery
5.Plexiform fibromyxoma of stomach: a distinctive benign tumor of gastric antrum.
Feng-hua WANG ; Zheng-rong CHEN ; Hui-lin NIU ; Rong-xin ZENG ; Jian-qing XIA
Chinese Journal of Pathology 2012;41(3):190-191
Actins
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immunology
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metabolism
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Antibodies, Monoclonal
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metabolism
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Child
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Diagnosis, Differential
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Fibroma
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metabolism
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pathology
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surgery
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Follow-Up Studies
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Gastrointestinal Neoplasms
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metabolism
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pathology
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Gastrointestinal Stromal Tumors
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metabolism
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pathology
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Humans
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Leiomyoma
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metabolism
;
pathology
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Male
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Pyloric Antrum
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pathology
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Stomach Neoplasms
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metabolism
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pathology
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surgery
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Vimentin
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metabolism