1130-0108/2015/107/1/37-38 REVISTA ESPAÑOLA DE ENFERMEDADES DIGESTIVAS REV ESP ENFERM DIG (Madrid COPYRIGHT © 2015 ARÁN EDICIONES, S. L. Vol. 107, N.º 1, pp. 37-38, 2015 PICTURES IN DIGESTIVE PATHOLOGY Inflammatory fibroid polyp of the appendix or Vanek’s tumor Ángela Sánchez-Cifuentes1, Francisco Miguel González-Valverde2, Miguel Ruiz-Marín1, Emilio Peña-Ros1, María Vicente-Ruiz1, Nuria Martínez-Sanz1, Concepción Escamilla-Segade1, Francisco Pastor-Quirante3 and Antonio Albarracín-Marín-Blázquez2 1Department of Geranal Surgery and Digestive Diseases. Hospital General Universitario Reina Sofía. Murcia, Spain. Departments of 2Surgery and 3Pathology. Universidad de Murcia. Murcia, Spain CASE REPORT A 45 year old male with non-contributory past medical history presented to the emergency department with a chief complaint of acute right lower quadrant pain. On physical examination he was afebrile, with pain and tenderness in the right iliac fossa without signs of peritoneal irritation. Blood tests showed leukocytosis and neutrophilia. Abdominal ul- trasound reported a blind-ending, aperistalic, 12 mm tubular structure emanating from the cecum, consistent with a thick- walled appendix communicating at the tip with a 5x3 cm col- lection (Fig. 1). After preoperative diagnosis of appendiceal abscess secondary to acute appendicitis, the patient underwent laparoscopic surgery. A 5-cm diameter mass was found in the middle third of the appendix without any inflammatory signs, intraabdominal free fluid or damage at the base (Fig. 2), and a standard appendectomy was therefore performed. His- Fig. 2. Appendix laparoscopic image. tological examination revealed a proliferation of fibroblasts and capillary buds in edematous stroma with numerous eo- sinophilic polynuclear cells without atypia, consistent with appendiceal inflammatory fibroid polyp (Fig. 3). Fig. 3. Specimen macroscopic view: Tumor of well-defined limits with Fig. 1. Abdominal ultrasound: Appendiceal thickened wall communicating a necrotic center. The appendiceal wall appears atrophic with lumen with collection. obliteration (arrow). 38 A. SÁNCHEZ-CIFUENTES ET AL. REV ESP ENFERM DIG (MADRID) DISCUSSION Inflammatory fibroid polyp (IFP) or Vanek’s tumor is a rare benign submucosal tumor composed of fibrous connective tissue and inflammatory cells, especially eosinophils (1). Although IFPs can be found anywhere in the digestive tract, most are found in the stomach (2). They are usually asymptomatic; however, the clinical presentation varies depending on the size and location of the lesion (4). Endoscopic resection is the (standard) treatment of choice; otherwise, open or laparoscopic surgery could be necessary according to its size and location. Recurrence is very infrequent after complete resection and additional treatments are not required (2). This case exemplifies the difficulty in diagnosing this condition: A seemingly straightforward case of appendicitis in a male turned out to be a surprising discovery of IFP. Most commonly, these benign lesions occur in the gastric antrum, the small bowel and the cecum. Even more rarely they can occur in the appendix (5). Vanek’s appendiceal tumor is extremely rare and, according to our search, this could be the first reported case in the Spanish literature. REFERENCES 1. Morales Fuentes GA, Ariño Suarez M, Zarate Osorno A, Rodriguez Jerkov J, Terrazas Espitia F, Perez Manauta J. Polipo de Vanek o polipo fibroide inflamatorio. Informe de un caso y revisión de la literatura. Cir Cir 2011;79:263-7. 2. Ortiz Moyano C, Martínez García RC, Sánchez Muñoz D, Romero Gómez. Pólipo fibroide inflamatorio gástrico. Rev Esp Enferm Dig 2010;102:217-22. 3. Rosai J. Surgical Pathology. 9th Ed. Elsevier; 2004. p. 659-60. 4. Kordzadeh A. Vanek’s tumour mimicking an acute appendicitis. Int J Surg Case Rep 2011;2(8):264-6. REV ESP ENFERM DIG 2015; 107 (1): 37-38.