Journals / Bakırköy Tıp Dergisi / 2016 / Cilt: 12 - Sayı: 4

A case of jejunal fibromatosis treatment with using laparoscopic surgery

Laparoskopik Cerrahi İle Tedavi Edilen Jejunal Fibromatozis Olgusu

Pages
221–223
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In these type of cases safe margins can be achieved with wide laparoscopic excision.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Fibromatosis is the most common primary tumor of mesentery.
📊
Key Findings & Data:Herein, we presented a case who was 45 years old, complained of left lower quadrant pain.
💡
Conclusion & Impact:In these type of cases safe margins can be achieved with wide laparoscopic excision.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Fibromatosis is the most common primary tumor of mesentery. Mesenteric fibromatosis is a very rare lesion which does not metastasise but can be locally aggressive. Fibromatosis may be classified as extra-abdominal, abdominal wall, or intra-abdominal. The etiology of fibromatosis has not been determined. Most of the patients with mesenteric fibromatosis are asymptomatic. Herein, we presented a case who was 45 years old, complained of left lower quadrant pain. Preoperative evaluation included abdominal ultrasound, computed tomography (CT). According to the CT report, the patient was diagnosed with gastrointestinal stromal tumor. A mobile mass was seen on the jejunal mesentery during laparoscopic exploration. The tumor was removed by wide excision with safe margins. Patients was discharged on the fifth day of the operation. The histological diagnosis was of jejunal agressive fibromatosis. Even though there are different types of treatment protocols, surgery with negative surgical margin is preferred to prevent local recurrence. In these type of cases safe margins can be achieved with wide laparoscopic excision.

Özet

Fibromatozis, mezenterin en sık görülen primer tümörüdür. Mezenterik fibromatozisler nadir görülen metastaz yapmayan ancak lokal olarak agresif özellik gösteren tümörlerdir. Yerleşim olarak ekstraabdominal, abdominal duvar ve intraabdominal olarak sınıflandırılabilir. Etiyolojisi tam olarak anlaşılamamıştır. Mezenterik fibromatozis hastaların büyük çoğunluğu asemptomatiktir. Burada karın ağrısı şikayeti ile başvuran 45 yaşındaki hastanın sunulması amaçlanmıştır. Ameliyat öncesi dönemde abdominal ultrasonografi ve abdominal tomografi ile değerlendirme yapıldı. Tomografi sonucuna göre hastaya ince barsak kaynaklı gastrointestinal stromal tümör tanısı kondu. Laparoskopik eksplorasyonda jejunum mezosundan köken alan mobil kitle saptandı. Tümör temiz cerrahi sınır ile geniş bir şekilde çıkartıldı. Hasta ameliyat sonrası 5. günde taburcu edildi. Histopatolojik olarak jejunal agresif fibromatozis tanısı kondu. Tedavide farklı protokoller olmasıyla birlikte lokal nüks riski açısından negatif cerrahi sınırla yapılan rezeksiyon ön planda görülen tedavi şeklidir. Bu olgularda laparoskopik teknikle geniş rezeksiyon uygulayarak temiz cerrahi sınırlarla kitle eksize edilebilir.

🔖

Cite This Article

BİLECİK, T., MAYIR, B., ORUÇ, T., ERYILMAZ, R. (2016). A case of jejunal fibromatosis treatment with using laparoscopic surgery. Bakırköy Tıp Dergisi, Cilt: 12 - Sayı: 4, 221–223. https://ajindex.com/articles/128658

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Reitamo JJ, Hayry P, Nykyri E, Saxen E. The desmoid tumor. I. incidence, sex, age and anatomical distribution in the Finnish population. Am J Clin Pathol 1982; 77: 665-673.
  2. Shields CJ, Winter DC, Kirwan WO, Redmond HP. Desmoid tumours. Eur J Surg Oncol 2001; 27: 701-706.
  3. Smith AJ, Lewis JJ, Merchant NB, Leung HY, Woodruff JM, Brennan MF. Surgical management of intraabdominal desmoid tumors. Br J Surg 2000; 87: 608-613.
  4. Bar-Maor JA, Shabshin U: Mesenteric fibromatosis. J Pediatr Surg 1993; 28: 1618-1619.
  5. Chanco G, Rose EF. Mesenteric fibromatosis following colectomy for familial polyposis. Arch Surg 1972; 104: 851-852.
  6. Shinagare AB, Ramaiya NH, Jagannathan JP, et al. A to Z of desmoid tumors. AJR Am J Roentgenol 2011; 197: W1008-W1014. Weiss SW, Goldblum JR. Fibromatosis. In: Marc Strauss (Ed). Enzinger's Soft Tissue Tumors, 4th edition. St Louis: Mosby; 2001: pp. 309-346.
  7. Yantiss RK, Spiro IJ, Compton CC, Rosenberg AE. Gastrointestinal stromal tumor versus intra-abdominal fibromatosis of the bowel wall. Am J Surg Pathol 2000; 24: 947-957.
  8. Miettinen M, Monihan JM, Sarlomo-Rikala M, et al. Gastrointestinal stromal tumors/smooth muscle tumors (GISTs) primary in the omentum and mesentery: clinicopathologic and immunohistochemical study of 26 cases. Am J Surg Pathol 1999; 23: 1109-1118.
  9. Faria SC, Iyer RB, Rashid A, Ellis L, Whitman GJ. Desmoid tumor of the small bowel and the mesentery. AJR Am J Roentgenol 2004; 183: 118. Brooks AP, Reznek RH, Nugent K, Farmer KC, Thomson JP, Phillips RK. CT Appearances of desmoid tumours in familial adenomatous polyposis: further observations. Clin Radiol 1994; 49: 601-607.
  10. Healy JC, Reznek RH, Clark SK, Phillips RK, Armstrong P. MR appearances of desmoid tumors in familial adenomatous polyposis. AJR Am J Roentgenol 1997; 169: 465-472.
  11. Al-Nafussi A, Wong NACS. Intra-abdominal spindle cell lesions: a review and practical aids to diagnosis. Histopathology 2001; 38: 387-402.
  12. Fletcher CDM, Berman JJ, Corless C, et al. Diagnosis of gastrointestinal stromal tumors: A Consensus approach. Hum Pathol 2002; 33: 459- 465. Miettenen M, Lasota J. Gastrointestinal stromal tumors-definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis. Virchows Arch 2001; 438: 1-12.
  13. Nuyttens JJ, Rust PF, Thomas CR, Turrisi AT. Surgery versus radiation therapy for patients with aggressive fibromatosis or desmoid tumors: A comparative review of 22 articles. Cancer 2000; 88: 1517- 1523.