Sep 2026· Global Journal of Medical and Clinical Case Reports· pp. 199-201· 0 citations· 2 references
TL;DR
The management of giant abdominal wall desmoid tumors with mass effect requires a personalized, multidisciplinary approach, oscillating between monitoring, medical alternatives, and salvage surgery.
Abstract
Desmoid tumors, or aggressive fibromatoses, are rare fibroblastic proliferations of soft tissues. Although benign from a metastatic standpoint, they possess a high potential for local invasion. Giant forms, inducing a compressive mass effect, pose complex therapeutic challenges. This case report highlights the critical decision-making process in giant abdominal wall desmoid tumors where immediate salvage surgery takes precedence over conservative active surveillance due to severe symptoms and tissue compression. We report the case of a 46-year-old female patient presenting with a large mass on the abdominal wall evolving over 6 months, causing chronic pain, functional impairment, and a significant mass effect on adjacent pelvic structures. Magnetic resonance imaging (MRI) revealed a large infiltrating tissue lesion. Biopsy and immunohistochemistry confirmed the diagnosis of aggressive fibromatosis. Given the significant mass effect, wide surgical excision with tumor-free margins was performed. The postoperative course was uneventful, with no local recurrence at the 6-month follow-up. Conclusion: The management of giant desmoid tumors with mass effect requires a personalized, multidisciplinary approach, oscillating between monitoring, medical alternatives, and salvage surgery.
Desmoid tumor (DT) is a rare mesenchymal neoplasm characterized by infiltrative and invasive growth with a tendency to recur. These tumors are locally aggressive and intermediate in behavior, with an incidence of two to five cases per million population. A 27-year-old female patient presented with an abdominal mass tha...
Germán Brito-Sosa, Ana María Iraizoz-Barrios· Revista de la Facultad de Me...· 0 citations
Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm that can occur in almost any anatomic site. Malignant SFT originating from the greater omentum is extremely rare. The Demicco risk-stratification system is commonly used to estimate postoperative recurrence and metastasis risk in patients with SFT. We repo...
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Inflammatory myofibroblastic tumor is a rare neoplasm. Its preferred location is intrathoracic; there are few reports of intra-abdominal involvement, where it may affect the mesentery and retroperitoneum. A 7-year-old girl was brought in for evaluation due to fever, nonspecific lower abdominal pain, fatigue, and progre...
Juan P. Pérez Rossini, Eugenia Perié, C. Soriano et al.· Archivos Argentinos de Pedia...· 0 citations
Introduction: Ovarian fibrothecal tumors are rare, benign neoplasms accounting for 1–4.7% of organic ovarian tumors, predominantly affecting postmenopausal women. This report highlights the diagnostic challenge and intraoperative management of a voluminous ovarian fibrothecal tumor presenting with atypical, purely mech...
Amine Chaabouni, M. Frikha, N. Kardoun et al.· International journal of sur...· 0 citations
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