Intussuception due to gastrointestinal stromal tumor with neural differentiation in a patient with Von Recklinghausen neurofibromatosis (NF-1): A case report
We document clinical and pathological aspects of a patient with Von Recklinghausen Neurofibromatosis presented with jejunojejunal intussuception due to a stromal tümör with neural differentiation.
📌 3 Key Takeaways
🎯
Objective & Hypothesis:Von Recklinghausen Neurofibromatosis is a fairly common disorder characterized with cafe au lait spots of the skin and neurofibromas of the skin and viscera.
📊
Key Findings & Data:Neurofibromas can be observed throughout the gastrointestinal tract and lead to various complications.
💡
Conclusion & Impact:We document clinical and pathological aspects of a patient with Von Recklinghausen Neurofibromatosis presented with jejunojejunal intussuception due to a stromal tümör with neural differentiation.
Von Recklinghausen Neurofibromatosis is a fairly common disorder characterized with cafe au lait spots of the skin and neurofibromas of the skin and viscera. Neurofibromas can be observed throughout the gastrointestinal tract and lead to various complications. These neurofibromas can be diagnosed with immunohistochemical studies in order to exclude other type of tumors. We document clinical and pathological aspects of a patient with Von Recklinghausen Neurofibromatosis presented with jejunojejunal intussuception due to a stromal tümör with neural differentiation.
Özet
Intussuception due to gastrointestinal stromal tumor with neural differentiation in a patient with Von Recklinghausen neurofibromatosis (NF-1): A case report
ÖZGÜDER, T., USLU, A., SELEK, E., KACAR, F., KOÇ, O. (2001). Intussuception due to gastrointestinal stromal tumor with neural differentiation in a patient with Von Recklinghausen neurofibromatosis (NF-1): A case report. Turkish Journal of Cancer, Cilt: 31 - Sayı: 4, 172–176. https://ajindex.com/articles/368430
Wallace MR, Marchuk DA, Andersen LB, et al. Type 1 neurofibromatosis gene: Identification of a large transcript distrupted in three NF-1 patients. Science 1990;249:181-2
Kheir SM, Halpern NB. Paraganglioma of the duodenum in association with congenital neurofibromatosis. Cancer 1984;53:2491-6
Angerpointer TA, Weitz H, Haas RJ. Intestinal leiomyosarcoma in childhood. Case report and review of the literature. J Pediatr Surg 1981;16:491-5
Mc Loughlin LC, Nord KS, Joshi W, et al. Disseminated leiomyosarcoma in a child with an acquired immune deficiency syndrome. Cancer 1991;67:2618- 21
Vallaeys JH, Cuvelier CA, Beckaert L, et al. Combined leiomyomatosis of the small intestine and colon. Arch Pathol Lab Med 1993;116:281-3
Franquement DW. Differentiation and risk assessment of gastrointestinal stromal tumors. Am J Clin Pathol 1995;103:41-7
Juan R. Gastrointestinal tract pathology. In: Ackerman Surgical Pathology. Mosby-Year book, Inc. 1996: 691-3
Inai K, Kobuke T, Yonehama S, et al. Duodenal gangliocytic paraganglioma with lymph node metastasis in a 17-year-old boy. Cancer 1989;63:2540-5
Mentzel T, Katenkamp D. Gastrointestinal stromal tumor with skenoid fibres and bidirectional immunohistochemical differentiation. Histopathology 1996;29:175-7
Shanks JH, Marris M, Banerjee SS, et al. Gastrointestinal autonomic nerve tumors: A report of nine cases. Histopathology 1996;29:111-21
Min KW. Small intestinal stromal tumours with skenoid fibres. Clinicopathological, immunohistochemical and ultrastructural investigations. Am J Surg Pathol 1992;16:145-55
Segal A, Carello S, Caterina P, et al. Gastrointestinal autonomic nerve tumours: a clinicopathological, immunohistochemical and ultrastructural study of 10 cases. Pathology 1994;26:439-47
Newman PL, Wadden C, Fletcher CDM. Gastrointestinal stromal tumours: Correlation of immunophenotype with clinicopathological features. J Pathol 1991;164:107-17.