Inflammatory Myofibroblastic Tumor of the Larynx: Case Report

Benign Tumor ◽

Mesenchymal Origin

Inflammatory Myofibroblastic Tumor is usually a benign tumor of mesenchymal origin that is rarely found in the larynx. This case explores the unique laryngeal location and presentation of this tumor as well as the challenging radiographic and histologic findings.

Meninge inflammatory myofibroblastic tumor: rare case report and literature review

10.5327/1516-3180.133 ◽

2021 ◽

Author(s):

Ligia Henriques Coronatto ◽

Enzo Barnabé Monteiro ◽

Gabriel Novaes de Rezende Batistella ◽

Natália Silva Fernandes ◽

Adrialdo José Santos

Keyword(s):

Case Report ◽

Complementary Therapies ◽

Benign Tumor ◽

Medical Attention ◽

Main Challenge ◽

Complete Surgical Resection ◽

Rare Case Report ◽

The Central Nervous System ◽

The Ideal

Context: Inflammatory myofibroblastic tumor (IMT), also known as inflammatory pseudotumor or plasma cell granuloma is a benign tumor of mesenchymal origin that can occur in different anatomical locations, but is more common in the lung and liver, being rare in the central nervous system (CNS). The main challenge when finding this type of tumor in meninges is to make the differential diagnosis with metastatic neoplastic infiltration, granulomatous and infectious diseases. The ideal treatment is complete surgical resection, not requiring other complementary therapies due to its benign behavior. Case report: This work brings the case report of a 22-year-old young man who search medical attention due to headache and after extensive investigation presented the diagnosis of myofibroblastic tumor of the meninges. Conclusion: A comprehensive review of the literature on this type of tumor was carried out in this location, but with very few cases and papers written to date.

A rare benign tumor of the lung: Inflammatory myofibroblastic tumor – Case report

Respiratory Medicine Case Reports ◽

10.1016/j.rmcr.2013.01.001 ◽

2013 ◽

Vol 8 ◽

pp. 32-35

Author(s):

Ozkan Demirhan ◽

Selvinaz Ozkara ◽

Mustafa Yaman ◽

Kamil Kaynak

Keyword(s):

Case Report ◽

Benign Tumor ◽

Rare Benign Tumor

Inflammatory Myofibroblastic Tumor of Perineal Soft Tissue: A Case Report

Journal of the Korean Radiological Society ◽

10.3348/jkrs.2001.45.4.417 ◽

2001 ◽

Vol 45 (4) ◽

pp. 417

Author(s):

Jong Myeong Yang ◽

Kyu Soon Kim ◽

Soon Tae Kwon ◽

Jong Chul Kim ◽

Kyu Sang Song

Keyword(s):

Case Report ◽

Soft Tissue ◽

Primary inflammatory myofibroblastic tumor of the liver: case report

Kanzo ◽

10.2957/kanzo.53.272 ◽

2012 ◽

Vol 53 (5) ◽

pp. 272-277 ◽

Cited By ~ 1

Author(s):

Hisashi Kosaka ◽

Nobukazu Kuroda ◽

Norihiro Nakai ◽

Koichiro Ohashi ◽

Kazuhiro Suzumura ◽

...

Keyword(s):

Case Report ◽

An Invasive Hemolymphangioma of the Pancreas in a Young Woman

Combinatorial Chemistry & High Throughput Screening ◽

10.2174/1386207322666190103110747 ◽

2019 ◽

Vol 21 (10) ◽

pp. 798-800 ◽

Cited By ~ 1

Author(s):

Zhijun Zhang ◽

Qinghong Ke ◽

Weiliang Xia ◽

Xiuming Zhang ◽

Yan Shen ◽

...

Keyword(s):

Computed Tomography ◽

Case Report ◽

Young Woman ◽

Benign Tumor ◽

Abdominal Distension ◽

Accurate Diagnosis ◽

Cystic Tumor ◽

Rare Benign Tumor ◽

Radical Surgical Resection

Background: Hemolymphangioma is a rare benign tumor. To the best of our knowledge, there were only 10 reports of this tumor of the pancreas until March 2018. Case Report: Here, we reported a large invasive hemolymphangioma of the pancreas in a young woman with a complaint of abdominal distension and an epigastric mass about 3 weeks. She was found to have a huge multilocular cystic tumor at the neck and body of pancreas on computed tomography. She was eventually diagnosed with hemolymphangioma of the pancreas after operation. After 2 years of follow-up, there was no signs of recurrence. Conclusion: From our case and literature, we can conclude that hemolymphangioma of the pancreas is uncommon benign tumor, and it is hard to make an accurate diagnosis preoperatively. Radical surgical resection should be performed whenever possible. The prognosis of this disease seems good.

Testicular fibroma: A case report

Archive of oncology ◽

10.2298/aoo1304139s ◽

2013 ◽

Vol 21 (3-4) ◽

pp. 139-140

Author(s):

Sunita Shere ◽

Anjali Kulkarni ◽

Shubhjyoti Pore ◽

Rajan Bindu

Keyword(s):

Case Report ◽

Benign Tumor ◽

Histopathological Diagnosis ◽

Testicular Mass ◽

Rare Benign Tumor ◽

Testicular Malignancy ◽

Slow Growing

Testicular fibroma of gonadal stromal origin is a rare benign tumor of testis, which usually presents as a slow growing testicular mass. Intratesticular fibroma of gonadal stromal origin, with or without minor sex cord elements, must be considered, analogous to similar tumors in ovary, as a benign tumor. Until now, only 25 cases of testicular fibroma have been reported in the literature. We reported a case of testicular fibroma in a 20 years male who presented with painless right testicular enlargement since two years. Ultrasonography (USG) showed heterogeneous mass in right scrotum suggestive of testicular malignancy. Right orchidectomy was done. Histopathological diagnosis was testicular fibroma, which was confirmed by immunohistochemistry.

Case report of an unexpected inflammatory myofibroblastic tumor

Annals of Medicine and Surgery ◽

10.1016/j.amsu.2021.102316 ◽

2021 ◽

pp. 102316

Author(s):

Vishal Farid Raza ◽

Dawood Arshad ◽

Sajeel Ahmad ◽

Khalid Javeed Khan

Keyword(s):

Case Report ◽

Renal inflammatory myofibroblastic tumor: A case report

Urology Case Reports ◽

10.1016/j.eucr.2021.101620 ◽

2021 ◽

Vol 37 ◽

pp. 101620

Author(s):

A.S. Ivanov ◽

P.A. Antonov ◽

Z.R. Chitalov

Keyword(s):

Case Report ◽

INFLAMMATORY MYOFIBROBLASTIC TUMOR OF THE MEDIASTINUM: A RARE CASE REPORT

CHEST Journal ◽

10.1016/j.chest.2021.07.1175 ◽

2021 ◽

Vol 160 (4) ◽

pp. A1286

Author(s):

Arish Maknojia ◽

Raguraj Chandradevan ◽

Taniya Mathew ◽

Neeta Sukthanker

Keyword(s):

Case Report ◽

Rare Case ◽

Rare Case Report

Open Surgical Hip Dislocation for an Acetabular Osteoid Osteoma - A Case Report

Journal of Surgical Case Reports and Images ◽

10.31579/2690-1897/093 ◽

2022 ◽

Vol 5 (1) ◽

pp. 01-04

Author(s):

Parker J. Prusick ◽

Steven D. Jones ◽

Jesse Roberts ◽

Nathan Donaldson

Keyword(s):

Case Report ◽

Osteoid Osteoma ◽

Proximal Femur ◽

Benign Tumor ◽

Hip Dislocation ◽

Long Bones ◽

Surgical Hip Dislocation ◽

Sclerotic Bone

Osteoid osteoma is a benign tumor that accounts for roughly 10-12% of all benign bone forming tumors. This tumor generally occurs within the first three decades of life and occurs more commonly in males. This lesion is painful and is generally worse at night and has relief of symptoms with the use of NSAIDs. Osteoid osteoma is characterized by the production of osteoid surrounded by a rim of sclerotic bone. These lesions most commonly occur in long bones such as the proximal femur, however they can occur anywhere. Rarely, as with our patient, have these lesions been reported in the acetabulum.