期刊文献+

ALK阴性的胃炎性肌纤维母细胞瘤一例 被引量:3

原文传递
导出
摘要 患者男,19岁。无明显诱因出现黑便,伴有头晕,无呕血、恶心、呕吐等症状,感觉上腹饥饿不适,当时未引起重视,此后黑色烂便1~2次/天,每次约100~200 g,伴头晕、黑蒙、乏力。患者再次感头晕、恶心、上腹饱胀,呕血1次,暗红色,含血块、量多,约300 g,伴全身出汗,于2014年7月22日就诊于绍兴市人民医院。实验室检测:血常规:白细胞8.06×10^9/L,血红蛋白120 g/L,红细胞比容0.38,血小板161×10^9/L;腹部B超无特殊;粪常规:OB +++。临床考虑消化道出血,给予潘托拉唑针制酸及补液等对症治疗,患者病情好转,再无呕血。7月28日患者主诉黑色烂便一次,为了进一步明确诊治,急诊以“上消化道出血”收治。胃镜示胃大弯近胃底见一直径约40 mm隆起,其中间见一直径约20 mm的溃疡,表面覆白苔;超声内镜示病灶呈不均质回声团块,呈不规则形,向腔内外突出,边界欠清,起源于固有肌层。腹部CT示胃体部大弯侧见一结节状软组织影,直径27 mm,表面有凹陷,腹腔内未见明显异常的肿块影及异常高密度钙化影,盆腔内脏正常,腹腔内无积液,腹主动脉旁、腹膜后及盆壁内未见明显淋巴结肿大,影像学考虑胃肠道间质瘤伴溃疡。8月4日在全麻下行胃肿瘤切除术,术中见肿瘤位于胃体大弯近胃底处,大小约3.0 cm×4.0 cm,胃周未见明显淋巴结肿大。
出处 《中华病理学杂志》 CAS CSCD 北大核心 2015年第6期418-419,共2页 Chinese Journal of Pathology
基金 浙江省医学扶植重点建设学科计划(GJSX-010-004)
作者简介 魏建国,E-mail:mickmouse88@163.com
  • 相关文献

参考文献7

  • 1Qiu JF, Shi YJ, Fang L, et al. High fever as an initial symptom of primary gastric inflammatory myofibroblastic tumor in an aduh woman[J]. Int J Clin Exp Med, 2014,7(5) :1468-1473.
  • 2Katakwar A, Gedam BS, Mukewar S, et al. Primary gastric inflammatory myofibroblastic tumor in an adult-case report with brief review[J]. Indian J Surg Oncol, 2014, 5(1 ) :66-70.
  • 3方芳,李燕明,孙铭君,胡松涛,王征,刘冬戈,王辰.IgG4相关疾病的临床病理学特征[J].中华病理学杂志,2014,43(9):618-622. 被引量:14
  • 4李焕萍,沈勤,夏秋媛,时姗姗,章如松,余波,马恒辉,陆珍凤,王璇,何燕,周晓军,饶秋.肺外炎性肌纤维母细胞瘤的临床病理分析[J].中华病理学杂志,2014,43(6):370-374. 被引量:24
  • 5Coffin CM, Homick JL, Fletcher CD. Inflammatory myohbrobtasUc tumor: comparison of clinicopathologic, histdogic, and features including ALK expression in atypical and aggressive cases[J]. Am I Surg Pathol, 2007,31 (4) :509- 520.
  • 6Bjelovic M, Micev M, Spica B, et al. Primary inflammatory myofibroblastic tumor of the stomach in an adult woman: a case report and review of the literature[ J]. World J Surg Oncol, 2013, 11(1) :35-41.
  • 7Shi H, Wei L, Sun L, et al. Priwary gastric inflammatory myofibroblastic tumor: a clinicopathoIogic and immunohistochemical study of 5 cases[J]. Patho/IRes Pratt, 2010,206(5) :287-291.

二级参考文献3

共引文献36

同被引文献22

  • 1Choi KW, Lee WY, Hong SW, et al. Carcinosarcoma of the stomach: a case report[ J]. J Gastric Cancer, 2013, 13 ( 1 ) :69- 72. DOI : 10. 5230/jge. 2013.13.1.69.
  • 2Ciroechi R, Trastulli S, Desiderio J, et al. Gastric a case report and review of the literature [ J Oncol Lett, 2012, 4(1) :53-57.
  • 3Kamata K, Wada R, Yajima N, et al. Primary gastric synovial sarcoma : molecular diagnosis and prediction of prognosis[ J]. Clin J Gastroenterol, 2013, 6(4) :303-308. DOI: 10. 1007/s12328- 013-0403-0.
  • 4Miettinen M, Dow N, Lasota J, et al. A distinctive novel epitheliomesenchymal biphasic tumor of the stomach in young adults ( "gastroblastoma" ) : a series of 3 cases [ J ]. Am J Surg Pathol, 2009, 33 (9) : 1370-1377.
  • 5Shin DH, Lee JH, Kang H J, et al. Novel epitheliomesenchymal biphasic stomach tumour (gastroblastoma) in a 9-year-old: morphological, ultrastruetural and immunohistochemical findings [J].J Clin Pathol, 2010, 63(3) :270-274. DOI:10. l136/jcp. 2009. 074104.
  • 6] Wey EA, Britton AJ, Sferra JJ, et al. Gastroblastoma in a 28-year- old man with nodal metastasis: proof of the malignant potential [J]. Arch Pathol Lab Med, 2012, 136(8) :961-964. DOI:IO. 5858/arpa. 2011-0372-CR.
  • 7Ma Y, Zheng J, Zhu H, et al. Gastroblastoma in a 12-year-old Chinese boy[ J]. Int J Clin Exp Pathol, 2014, 7 (6) :3380-3384.
  • 8Fernandes T, Silva R, Devesa V, et al. AIRP best cases in radiologic-pathologic correlation: gastroblastoma: a rare biphasic gastric tumor [ J ]. Radiographics, 2014, 34 ( 7 ) : 1929-1933. DOI: 10. l148/rg. 347130103.
  • 9Kharga B, Kumar V, Prabhu PS, et al. Neonatal gastric teratoma : a rare entity[ J]. J Clin Diagn Res, 2014, 8 (1) :185-186. DOI: 10. 7860/JCDR/2013/7338. 3972.
  • 10Yaji PR, Joshi S, Kinhal V,et al. Gastric teratoma in an infant: a rare case report and discussion [ J ]. Indian J Surg, 2013, 75 (Suppl 1 ) : 152-154. DOI: 10. 1007/s12262..012-0568-7.

引证文献3

二级引证文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部