دورية أكاديمية
Splenic lymphangioma.
العنوان: | Splenic lymphangioma. |
---|---|
المؤلفون: | Ousmane T; General Surgery Department at Dalal Jamm Hospital, Dakar, Senegal. Electronic address: o_thiam@hotmail.fr., Mamadou FP; General Surgery Department at Aristide Le Dantec Hospital, Senegal., Sitor SI; General Surgery Department at Aristide Le Dantec Hospital, Senegal., Abdou N; General Surgery Department at Aristide Le Dantec Hospital, Senegal., Madieng D; General Surgery Department at Aristide Le Dantec Hospital, Senegal. |
المصدر: | International journal of surgery case reports [Int J Surg Case Rep] 2019; Vol. 62, pp. 40-42. Date of Electronic Publication: 2019 Aug 08. |
نوع المنشور: | Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 101529872 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2210-2612 (Print) Linking ISSN: 22102612 NLM ISO Abbreviation: Int J Surg Case Rep Subsets: PubMed not MEDLINE |
أسماء مطبوعة: | Original Publication: [Amsterdam] : Elsevier B.V. |
مستخلص: | Introduction: Abdominal localization of cyst lymphangioma is rare. The splenic involvement is exceptional. Case Presentation: A 63-year-old woman, who was followed for martial anemia evolving associated with abdominal pain in the past 12 months. On clinical examination, she had pallor conjunctival mucosa, with a normal abdominal and lymph node examination. The abdominal ultrasound showed multiple splenic cysts. The abdominal CT scan showed a normal-sized spleen with multiples hypodense cystic lesions. At the laparotomy exploration a multinodular spleen was found which measured 18 cm*15 cm*6 cm. The histological exam results showed concluded to a splenic cavernous lymphangioma without malignity signs. The follow-up after 12 months was normal. Conclusion: splenic lymphangioma is rare and benign tumor. Total splenectomy under laparotomy or laparoscopy is the appropriate treatment. (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.) |
References: | Semin Diagn Pathol. 2003 May;20(2):128-39. (PMID: 12945936) J Pediatr Surg. 1996 May;31(5):677-80. (PMID: 8861480) Rev Med Chil. 2004 Feb;132(2):189-94. (PMID: 15449555) Int J Surg. 2018 Dec;60:132-136. (PMID: 30342279) JSLS. 2001 Oct-Dec;5(4):313-6. (PMID: 11719977) J Chir (Paris). 2005 Jan-Feb;142(1):6-13. (PMID: 15883503) Ann Chir. 1994;48(1):7-16. (PMID: 8161161) Acta Cytol. 1994 May-Jun;38(3):299-309. (PMID: 8191816) Radiology. 1987 Aug;164(2):327-32. (PMID: 3299483) J Chir (Paris). 2008 May-Jun;145(3):238-43. (PMID: 18772731) Surg Innov. 2005 Mar;12(1):23-9. (PMID: 15846443) J Pediatr Surg. 1992 Feb;27(2):220-4; discussion 224-6. (PMID: 1564622) Surg Today. 2001;31(3):258-61. (PMID: 11318134) Arch Surg. 1985 Nov;120(11):1266-9. (PMID: 4051731) Magn Reson Imaging. 2003 Jan;21(1):81-4. (PMID: 12620551) Indian J Pathol Microbiol. 2005 Apr;48(2):202-3. (PMID: 16758665) Emerg Radiol. 2009 Jul;16(4):327-30. (PMID: 18604575) J Pediatr Surg. 2008 Jun;43(6):1206-8. (PMID: 18558209) Cir Cir. 2016 Mar-Apr;84(2):154-9. (PMID: 26242820) J Pediatr Surg. 1987 May;22(5):461-2. (PMID: 3585671) Surgery. 2000 Oct;128(4):660-7. (PMID: 11015100) J Gastrointest Surg. 2006 May;10(5):746-51. (PMID: 16713549) Gastroenterol Clin Biol. 1993;17(8-9):591-3. (PMID: 8253317) Am Surg. 1992 Oct;58(10):599-604. (PMID: 1416432) J Pediatr Hematol Oncol. 1997 May-Jun;19(3):232-6. (PMID: 9201146) Ann Chir. 2002 May;127(5):343-9. (PMID: 12094416) Diagn Cytopathol. 1997 Apr;16(4):312-6. (PMID: 9143823) Radiographics. 2004 Jul-Aug;24(4):1137-63. (PMID: 15256634) Rev Med Liege. 2010 Nov;65(11):615-8. (PMID: 21189526) Med Princ Pract. 2004 May-Jun;13(3):122-5. (PMID: 15073422) Ann Chir. 1993;47(6):553-6. (PMID: 8215185) |
فهرسة مساهمة: | Keywords: Lymphangioma; Rare; Splenic |
تواريخ الأحداث: | Date Created: 20190821 Latest Revision: 20240720 |
رمز التحديث: | 20240720 |
مُعرف محوري في PubMed: | PMC6717100 |
DOI: | 10.1016/j.ijscr.2019.07.078 |
PMID: | 31430605 |
قاعدة البيانات: | MEDLINE |
تدمد: | 2210-2612 |
---|---|
DOI: | 10.1016/j.ijscr.2019.07.078 |