YÜZEYSEL VE DERİN YERLEŞİMLİ FİBROMATOZİSLER: BENZER HİSTOMORFOLOJİK GÖRÜNÜM ANCAK FARKLI BİYOLOJİK DAVRANIŞ

Amaç: Fibromatozisler yüzeysel ya da derinyerleşimli olabilen ve çoğunlukla cerrahi eksizyon iletedavi edilen, lokal infiltratif yumuşak dokutümörleridir. Özellikle derin yerleşimlifibromatozislerin cerrahi ile lokal kontrolü sorun teşkiletmektedir. Bu çalışmada laboratuarımızdafibromatozis tanısı alan yüzeysel ve derin yerleşimliolguların klinik, histopatolojik ve immün boyanmaözellikleri karşılaştırılmıştır.Gereç ve yöntemler: Ocak 2005 ile Aralık 2013tarihleri arasında fibromatozis tanısı alan 12 olguçalışmaya alındı. Hastalarda yaş, cinsiyet, tümöryerleşimi, tümör boyutu, tümörlerin histomorfolojikve immün boyanma özellikleri karşılaştırıldı.İstatistiksel analizlerde Mann–Whitney U ve Chi-Square/Fisher's Exact testi kullanıldı. p < 0.05sonuçlar anlamlı kabul edildi.Bulgular: Fibromatozis tanısı alan olguların 4'üyüzeysel, 8'i derin yerleşimli idi. Hastaların yaşı 18 ile72 arasında değişmekteydi (ortalama 62,5). Yüzeyselyerleşimli olguların hepsi erkek, derin yerleşimliolguların hepsi kadındı. Yüzeysel yerleşimlitümörlerde nüks izlenmezken derin yerleşimliolgulardan 3'ü (%37,5) nüksetmişti. Yüzeyselyerleşimli tümörlerin boyutu 1,5 cm ile 4,5 cmarasında değişmekteydi (ortalama 3,5 cm). Derinyerleşimli tümörlerin boyutu 1,5 cm ile 15 cmarasında değişmekteydi (ortalama 9 cm). İstatistikselanalizde tümör lokalizasyonu ile cinsiyet (p= 0,002)ve tümör boyutu (p= 0,042) arasında anlamlı ilişkisaptandı. Tümör yerleşim yeri ile yaş (p= 0,173), nüksoranı (p= 0,491), desmin (p=0,491), düz kas aktin (p=0,091), S-100 protein (p=0,515), Ki-67 (p= 0,236)immün boyaları ve Ki-67 proliferasyon indeksi(p=0,248) arasında anlamlı ilişki görülmedi.Sonuç: Yüzeysel ve derin yerleşimli fibromatozislerinhistomorfolojik görünümü ve immün boyanmaözellikleri birbirine benzerdir. Ancak klinik özelliklerive biyolojik davranışları açısından bu iki antitebirbirinden farklı gibi gözükmektedir.

Superficial and Deep Situated Fibromatoses: Similar Histomorphologic Appearance but Different Biological Behavior

Aim: Fibromatoses are a locally infiltrative soft tissue tumors being situated superficial or deep tissues and usually treated by surgical excision. The surgical local control of these tumors, especially ones arising from deep tissues, remains a significant problem. On this study, we aimed to investigate the clinical, histopathological and immune staining features of superficial and deep fibromatoses diagnosed our laboratory. Material and methods: Consecutive twelve cases diagnosed as fibromatoses between January 2005 to December 2013 were included to the study. Patients' ages, sex, the localization of tumor, the tumor size, histomorphological features and immune staining profiles of tumors were investigated. Statistical analyses were performed using Mann–Whitney U and Chi-Square/Fisher's Exact test. Results were considered to be significant at p < 0.05. Results: Four cases were superficial-seated, and 8 cases were deep-seated fibromatoses. The age of patients ranged from 18 to 72 (mean 62.5). All of superficial fibromatoses were male. All of deep fibromatoses were female. No recurrence was observed on superficial tumors. Three (37.5%) of deep-seated tumors had recurrent. The size of superficial tumors ranged from 1.5 cm to 4.5 cm (mean: 3.5 cm). The size of deep-seated tumors ranged from 1.5 cm to 15 cm (mean: 9 cm). There was no statistically significant difference between the two groups, in terms of the patients' age (p= 0.173), the recurrence rate (p= 0.491), Ki-67 proliferation index (p = 0.248) and immune staining for desmin (p= 0.491), smooth muscle actin (p= 0.091), S-100 protein (p= 0.515), Ki-67 (p = 0.236). Statistically, a significant correlation was observed between the two groups, in terms of the gender (p= 0.002) and the tumor size (p= 0.042). Conclusion: The histomorphological appearance and immune staining characteristics of superficial and deep-seated fibromatoses are similar. However, the clinical features and in terms of biological behavior of these two entities seems to be different from each other

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  • Kruse AL, Luebbers HT, Grätz KW, Obwegeser JA. Aggressive fibromatosis of the head and
  • neck: a new classification based on a literature review over 40 years (1968–2008). Oral and
  • maxillofacial surgery. 2010;14(4):227-32.
  • Salas S, Dufresne A, Bui B, Blay J-Y, Terrier P, Ranchere-Vince D, et al. Prognostic factors
  • influencing progression-free survival determined from a series of sporadic desmoid tumors: a waitand-
  • see policy according to tumor presentation. Journal of Clinical Oncology. 2011;29(26):3553-8.
  • Stout AP. Juvenile fibromatoses. Cancer. 1954;7(5):953-78.
  • Kreuzberg B, Koudelova J, Ferda J, Treska V, Spidlen V, Mukensnabl P. Diagnostic problems
  • of abdominal desmoid tumors in various locations. European journal of radiology. 2007;62(2):180-5.
  • Molloy A, Hutchinson B, O'Toole G. Extra-abdominal desmoid tumours: a review of the
  • literature. Sarcoma. 2012;2012.
  • Bonvalot S, Eldweny H, Haddad V, Rimareix F, Missenard G, Oberlin O, et al. Extraabdominal
  • primary fibromatosis: aggressive management could be avoided in a subgroup of patients.
  • European Journal of Surgical Oncology (EJSO). 2008;34(4):462-8.
  • Stoeckle E, Coindre J, Longy M, Bui Nguyen Binh M, Kantor G, Kind M, et al. A critical
  • analysis of treatment strategies in desmoid tumours: a review of a series of 106 cases. European
  • Journal of Surgical Oncology (EJSO). 2009;35(2):129-34.
  • Tolan S, Shanks J, Loh M, Taylor B, Wylie J. Fibromatosis: benign by name but not
  • necessarily by nature. Clinical Oncology. 2007;19(5):319-26.
  • El-Haddad M, El-Sebaie M, Ahmad R, Khalil E, Shahin M, Pant R, et al. Treatment of
  • aggressive fibromatosis: the experience of a single institution. Clinical Oncology. 2009;21(10):775-80.
  • Mullen JT, DeLaney TF, Kobayashi WK, Szymonifka J, Yeap BY, Chen Y-L, et al. Desmoid
  • tumor: analysis of prognostic factors and outcomes in a surgical series. Annals of surgical oncology.
  • ;19(13):4028-35.
  • Bertani E, Testori A, Chiappa A, Misitano P, Biffi R, Viale G, et al. Recurrence and
  • prognostic factors in patients with aggressive fibromatosis. The role of radical surgery and its
  • limitations. World Journal of Surgical Oncology. 2012.
  • Escobar C, Munker R, Thomas JO, Li BD, Burton GV. Update on desmoid tumors. Annals of
  • Oncology. 2012;23(3):562-9.
  • Catton C, O'Sullivan B, Bell R, Cummings B, Fornasier V, Panzarella T. Aggressive
  • fibromatosis: optimisation of local management with a retrospective failure analysis. Radiotherapy and
  • Oncology. 1995;34(1):17-22.
  • Colombo C, Gronchi A. Desmoid-type fibromatosis: What works best? European Journal of
  • Cancer. 2009;45:466-7.
  • Ozger H, Eralp L, Toker B, Agaoglu F, Dizdar Y. Evaluation of prognostic factors affecting
  • recurrences and disease-free survival in extra-abdominal desmoid tumors. Acta Orthop Traumatol
  • Turc. 2004;41(4):291-4.
  • Sleijfer S. Management of aggressive fibromatosis: Can we unravel the maze of treatment
  • options? European Journal of Cancer. 2009;45(17):2928-9.
  • Quintini C, Ward G, Shatnawei A, Xhaja X, Hashimoto K, Steiger E, et al. Mortality of intraabdominal
  • desmoid tumors in patients with familial adenomatous polyposis: a single center review of
  • patients. Annals of surgery. 2012;255(3):511-6.
  • Ioannidis O, Paraskevas G, Chatzopoulos S, Kotronis A, Papadimitriou N, Konstantara A, et
  • al. Multiple desmoid tumors in a patient with familial adenomatous polyposis caused by the novel
  • W421X mutation. Revista espanola de enfermedades digestivas: organo oficial de la Sociedad
  • Espanola de Patologia Digestiva. 2012;104(3):146-50.
  • Huss S, Nehles J, Binot E, Wardelmann E, Mittler J, Kleine MA, et al.
  • β‐Catenin(CTNNB1)mutations and clinicopathological features of mesenteric desmoid‐type
  • fibromatosis. Histopathology. 2013;62(2):294-304.
  • Kohli K, Kawatra V, Khurana N, Jain S. Multicentric synchronous recurrent aggressive
  • fibromatosis. Journal of Cytology. 2012;29(1).
  • Kempson R, Fletcher C, Evans H, Hendrickson M, Sibley R. Atlas of tumor pathology.
  • Tumors of the soft tissues Washington, DC: AFIP. 2001.
  • Rüdiger HA, Ngan SY, M N, GJ P, PF C. Radiation therapy in the treatment of desmoid
  • tumours reduces surgical indications. Eur J Surg Oncol 2010(36):84–8.
  • Gluck I, Griffith KA, Biermann JS, Feng FY, Lucas DR, Ben-Josef E. Role of Radiotherapy in
  • the Management of Desmoid Tumors International Journal of Radiation Oncology, Biology, Physics.
  • ;80(3):787-92.
  • Gounder MM, Lefkowitz RA, Keohan ML, D’Adamo DR, Hameed M, Antonescu CR, et al.
  • Activity of Sorafenib against Desmoid Tumor/Deep Fibromatosis. Clinical Cancer Research.
  • ;17(12):4082–90.
  • Constantinidou A, Jones RL, Scurr M, Al-Muderis O, Judson I. Pegylated liposomal
  • doxorubicin, an effective, well-tolerated treatment for refractory aggressive fibromatosis. European
  • Journal of Cancer. 2009;45(17):2930-4.
  • de Camargo VP, Keohan ML, D'Adamo DR, Antonescu CR, Brennan MF, Singer S, et al.
  • Clinical outcomes of systemic therapy for patients with deep fibromatosis (desmoid tumor). Cancer.
  • ;116(9):2258-65.
  • Baumert BG, Spahr MO, Von Hochstetter A, Beauvois S, Landmann C, Fridrich K, et al. The
  • impact of radiotherapy in the treatment of desmoid tumours. An international survey of 110 patients.
  • A study of the Rare Cancer Network. Radiat Oncol. 2007;2(1):12.
Interdisciplinary Medical Journal-Cover
  • Yayın Aralığı: Yılda 3 Sayı
  • Başlangıç: 2023
  • Yayıncı: Hatay Mustafa Kemal Üniversitesi Tıp Fakültesi Dekanlığı