32 results match your criteria fibroma ascending


Paucicellular Fibroma of the Ascending Aorta.

Aorta (Stamford) 2021 Oct 12. Epub 2021 Oct 12.

Department of Cardiovascular and Thoracic Surgery, Zucker School of Medicine at Hofstra/Northwell, Manhasset, New York.

Primary tumors of the aorta are extremely rare. To the best of our knowledge, herein, we present the first case in the literature of a paucicellular fibroma originating from the aortic wall. Read More

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October 2021

Intra-abdominal Desmoid-Type Fibromatosis Mimicking Diverticulitis With Abscess: A Case Report.

In Vivo 2021 Mar-Apr;35(2):1151-1155

The Department of Surgery, Kyusyu Central Hospital of the Mutual Aid Association of Public School Teachers, Fukuoka, Japan.

Background: Intra-abdominal desmoid-type fibromatosis (DF) rarely necessitates emergency surgery. However, the condition is difficult to diagnose preoperatively and can become life-threatening if left untreated.

Case Report: A 46-year-old man complained of fever and right lower quadrant pain. Read More

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Papillary Fibroelastoma of the Ascending Aorta.

J Investig Med High Impact Case Rep 2019 Jan-Dec;7:2324709619840377

2 Geisinger Medical Center, Danville, PA, USA.

Papillary fibroelastomas are rare benign primary cardiac tumors. They are typically found on valvular surfaces, most commonly, the aortic valve. In this article, we report a case of papillary fibroelastoma arising from the sinotubular junction of the ascending aorta, a rare and unusual site causing an embolic stroke. Read More

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[Papillary Fibroelastoma of the Pulmonary Valve;Report of a Case].

Kyobu Geka 2018 10;71(11):965-968

Department of Cardiovascular Surgery, Shin-Koga Hospital, Kurume, Japan.

We herein present a rare case of a papillary fibroelastoma on the pulmonary valve. A 66-year-old female underwent a graft replacement of the ascending aorta and an aortic valve replacement. Subsequent biannual checks have been performed as a follow up to surgery. Read More

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October 2018

Metachronous ameloblastic fibro-odontoma and dentigerous cyst in the posterior mandible.

Gen Dent 2017 Nov-Dec;65(6):69-72

An ameloblastic fibro-odontoma (AFO) is a rare mixed odontogenic tumor with histologic features of an ameloblastic fibroma in conjunction with the presence of dentin and enamel. It usually appears as a well-circumscribed radiolucency with radiopaque foci and slow growth and is commonly seen in children and young adults. A 13-year-old boy presented with an asymptomatic swelling in the posterior right region of the mandible and the right ascending ramus. Read More

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Central Odontogenic Fibroma of the Mandible.

J Dent Child (Chic) 2016 ;83(2):94-7

Department of Oral and Maxillofacial Pathology, Mamata Dental College, Khammam, Telangana, India.

The central odontogenic fibroma (COF) is a benign odontogenic tumor of mesenchymal tissue such as the periodontal ligament, dental papilla or dental follicle. It is an extremely rare tumor, accounting less than five percent of all odontogenic tumors. In this report, we describe the case of an eight year old girl who presented with a painless swelling of the left mandible. Read More

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November 2017

Aggressive multilocular osteoblastoma in the mandible: a rare and difficult case to diagnose.

Braz Dent J 2014 Sep-Oct;25(5):451-6

Universidade Estadual da Paraíba, Campina Grande, PB, Brazil.

Osteoblastoma is a benign neoplasia and is uncommon in the jaws. In some cases, this lesion presents extremely aggressive local characteristics and is termed aggressive osteoblastoma. Because the clinical, radiographic and histopathologic characteristics are similar to those of a variety of benign and malignant tumors, it poses a diagnostic dilemma. Read More

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November 2016

Desmoid tumour (aggressive fibromatosis) of the colon mimics malignancy on dual time-point 18F-FDG PET/CT imaging.

Br J Radiol 2012 Feb;85(1010):e37-40

Department of Nuclear Medicine, Brandon Regional Health Centre, Brandon, MB, Canada.

A 58-year-old female who presented with a lower gastrointestinal bleed was referred for an (18)F-fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT after a colonoscopy revealed a submucosal mass in the ascending colon. The PET/CT confirmed the presence of an FDG-avid mass in the ascending colon with no other FDG-avid abnormalities. Dual time-point imaging was performed and showed a significant increase in FDG uptake in the mass, which raised strong suspicion of a colon malignancy. Read More

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February 2012

[A case reported of an ameloblastic fibroma in which involved three right molars in a teenager].

Rev Med Inst Mex Seguro Soc 2011 May-Jun;49(3):339-44

Hospital General de Zona 1, Tepic, Nayari, Instituto Mexicano del Seguro Social, Mexico.

Ameloblastic fibroma is a benign tumor of mixed odontogenic origin, which occurs in ages from 12 to 15 years, frequently in the molar area. Generally it is asymptomatic, however the biggest lesions can be associated to pain and swelling. Using X-ray they appear well defined, transparent, with a sclerotic radio-opaque border; occasionally they can simulate a dentigerous cyst. Read More

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September 2011

[Sporadic case of desmoid tumor in outcomes of lombotomic nephrectomy].

Urologia 2011 Jul-Sep;78(3):206-9

Divisione di Urologia, Fondazione Poliambulanza, Brescia, Italy.

Unlabelled: The desmoid tumor is a rare tumor with an incidence of 2-4 cases per million people each year, and represents 0.03% of all cancers. The tumor is composed of fibrous tissue that produces masses of well-differentiated hard elastic consistency. Read More

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February 2012

Intra-abdominal desmoid tumor mimicking locoregional recurrence after colectomy in a patient with sporadic colon cancer: report of a case.

Surg Today 2011 May 1;41(5):730-2. Epub 2011 May 1.

Gastroenterological Center, Department of Gastroenterological Surgery, Cancer Institute Hospital, 3-10-6 Ariake, Koto-ku, Tokyo, 135-8550, Japan.

Desmoid tumors are rare, benign fibromatous lesions that result from the abnormal proliferation of myofibroblasts. A 61-year-old man underwent laparoscopy-assisted right hemicolectomy for ascending colon cancer. The final TNM stage was stage IIIB (T3N1M0). Read More

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Intraluminal ascending aorta fibroma.

J Tehran Heart Cent 2011 28;6(1):45-7. Epub 2011 Feb 28.

Shaheed Rajaei Cardiovascular Medical and Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Primary cardiac tumors are quite rare, especially in the pediatric age group, and their atypical presentations often prevent a timely diagnosis. Most primary cardiac tumors in the pediatric age group are benign. Fibromas are generally reported as the second most common primary cardiac tumors in the pediatric age group. Read More

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October 2012

A papillary fibroelastoma of the aortic valve that presented with repeated chest pain.

Gen Thorac Cardiovasc Surg 2010 Dec 18;58(12):630-2. Epub 2010 Dec 18.

Division of Thoracic and Cardiovascular Surgery, Niigata Prefectural Shibata Hospital, 1-2-8 Honcho, Shibata, Niigata, 957-8588, Japan.

A 70-year-old woman without any previous history of heart disease was referred to our hospital for repeated chest discomfort. She had experienced temporary hemiparesis because of a cerebral infarction of unknown etiology. Clinical evaluations were all within normal limits except for echocardiography. Read More

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December 2010

Incidentally diagnosed unusual ascending aorta mass.

Echocardiography 2011 Feb 27;28(2):E34-5. Epub 2010 Aug 27.

Department of Cardiology, Dr. Siyami Ersek Cardiovascular and Thoracic Surgery Training and Research Hospital, Istanbul, Turkkey.

A 44-year-old female, with no medical history, was admitted to the cardiology department because of mild exertional dyspnea. Transthoracic and transesophageal echocardiography showed highly mobile, mass-like lesion in the aortic root. The patient was operated in the same week and a 1 cm × 6 cm soft tissue was excised from the ascending aorta. Read More

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February 2011

Acute myocardial infarction caused by coronary embolization of a papillary fibroelastoma of the thoracic ascending aorta.

Interact Cardiovasc Thorac Surg 2010 Nov 25;11(5):676-7. Epub 2010 Aug 25.

Department of Cardiovascular Surgery, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne, Switzerland.

Papillary fibroelastomas (PFE) are benign endocardial masses and generally originate from the cardiac valves, while PFE arising from the ascending thoracic aorta are an uncommon clinical finding. We report the case of a 78-year-old female who presented to the emergency department with an acute ST segment elevation myocardial infarction. Urgent coronary angiography showed no significant coronary artery obstructive disease but left ventriculography revealed the presence of a highly mobile mass located in the proximal portion of the ascending thoracic aorta. Read More

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November 2010

Calcifying aponeurotic fibroma with bone islands exhibiting hematopoiesis: a case report and review of the literature.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010 Jun;109(6):878-82

Oral and Maxillofacial Pathology, Department of Dental Medicine, Long Island Jewish Medical Center, New Hyde Park, New York 11040, USA.

Aponeurotic fibroma (AF) was originally described by Keasbey in 1953 as juvenile aponeurotic fibroma, most commonly occurring in the distal extremities. Initially described in children and adolescents, AF is now recognized to occur over a wide age range and at various anatomic sites. A variant of this lesion, termed calcifying aponeurotic fibroma (CAF) has been described. Read More

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Rapid development of a papillary fibroelastoma in the aortic valve: report of a case.

Surg Today 2009 29;39(8):713-6. Epub 2009 Jul 29.

Department of Cardiovascular Surgery, Otemae Hospital, Chuo-ku, Osaka, Japan.

We report a case of a fast-growing cardiac papillary fibroelastoma (CPF) arising in the aortic valve. A 71-year-old woman was referred to a cardiologist for investigation of palpitations. Cardiac catheterization, coronary angiography, and echocardiography showed no stenosis of the coronary arteries, nor any other cardiovascular abnormalities. Read More

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September 2009

[Aggressive intraabdominal fibromatosis].

Vojnosanit Pregl 2006 Sep;63(9):839-42

Klinicki centar Srbije, Prva hirurska klinika, Institut za bolesti digestivnog sistema, Beograd.

Background: Intraabdominal or mesenteric fibromatosis is a rare benign nonmetastatic neoplasm that appears as a sporadic lesion or in patients with familiar polyposis. Its evolution is unpredictable. About 10% of the cases shaw a very aggressive growth. Read More

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September 2006

Ameloblastic fibroma: a case report in a 6 year old.

J Clin Pediatr Dent 2001 ;25(3):245-8

Department of Oral Pathology, Faculty of Medicine, School of Dentistry, Oviedo University, Astrurias, Spain.

A six-year-old boy was seen by his dentist for a tumor mass in the left mandibular region. The panograph revealed a multilocular radiotransparent lesion extending from the canine to the left mandibular ascending ramus with well defined borders. After biopsy, the lesion was enucleated via curettage of the bone bed. Read More

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Vascular complications associated with a large cardiac fibroma.

Eur J Cardiothorac Surg 2001 Sep;20(3):636-8

Cardiac Surgery Department, 'San Giovanni Battista' Hospital, Turin, Italy.

A case is reported of a 30-year-old patient with an intrapericardial tumour with heart failure. After the diagnostic protocol, surgery was performed initially without extra-corporeal circulation (ECC). Due to the location, size and to the large connection with the most important vascular structures, the ascending aorta ruptured accidentally during resection and was replaced after using ECC in emergency. Read More

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September 2001

Life-threatening giant mediastinal goiter: a surgical challenge.

J Cardiovasc Surg (Torino) 2001 Jun;42(3):429-30

Department of Thoracic Surgery, European Institute of Oncology, Milan, Italy.

Mediastinal goiter is a well known benign disease, usually resectable through a cervical approach with minimal morbidity and mortality. Only occasionally a median sternotomy or a lateral thoracotomy may be required. The present case is worthy of presentation because of the exceptional dimension of the disease and the surgical challenge that it presented. Read More

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Central fibroma in the ascending ramus of the mandible. Case report.

Aust Dent J 1999 Jun;44(2):131-4

Department of Oral Surgery, School of Medicine, Gunma University, Japan.

A case of central fibroma involving the mandible in a 58 year old woman is described. There was slight swelling of the left cheek and bone-hard bulging was detected on palpation but the patient had not complained of the swelling. The lesion was removed under general anaesthesia and then examined histopathologically. Read More

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Mandibular reconstruction using the anterior part of ascending ramus: report of two cases.

Authors:
T Muto M Kanazawa

J Oral Maxillofac Surg 1997 Oct;55(10):1152-6

First Department of Oral and Maxillofacial Surgery, School of Dentistry, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Japan.

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October 1997

Papillary fibroelastoma of the aortic valve in a patient with an acute myocardial infarction.

J Am Soc Echocardiogr 1996 Nov-Dec;9(6):897-900

Department of Cardiology, Sint Elisabeth Ziekenhuis, Tilburg, The Netherlands.

We describe a patient with a myocardial infarction in whom a tumor near the aortic valve was identified by routine transthoracic echocardiography. Transesophageal echocardiography proved to be particularly useful in identifying the attachment of the tumor to the aortic valve and enabled a surgical approach through the ascending aorta. On microscopic examination, the tumor appeared to be a papillary fibroelastoma. Read More

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February 1997

[A case report of surgical treatment for left ventricular papillary fibroelastoma].

Nihon Kyobu Geka Gakkai Zasshi 1996 Aug;44(8):1159-62

Department of Surgery II, Kochi Medical School, Japan.

A case of surgical treatment for left ventricular papillary fibroelastoma was reported. The patient was 75-year-old male who was admitted with complete A V block. Transesophageal echocardiogram revealed a mobile rounded mass (15 mm x 15 mm) in the LV attached to the IVS. Read More

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Fibromatosis--a rare retroperitoneal tumour.

Langenbecks Arch Chir 1990 ;375(1):51-4

Department of General Surgery, Karl-Franzens University, Medical School, Graz, Austria.

A case of retroperitoneal fibromatosis in a 28-year-old white male is presented. The soft tissue tumor, with a weight of 8000 g, was resected by laparotomy. Because of adhesions to the ascending colon and the right ureter, a hemicolectomy and partial resection of the right ureter had to be performed additionally. Read More

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Two cases of simple bone cyst suspected of being odontogenic tumors.

Aichi Gakuin Dent Sci 1989 ;2:9-17

We report here two cases of simple bone cyst suspected of odontogenic tumors. The first case, a 17-year-old female, was introduced to our department by a dental practitioner because of a large radiographic defect of the bone. The patient had no subjective symptoms. Read More

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September 1990

Aneurysmal bone cyst of the jaws. (I). Clinicopathological features.

Int J Oral Surg 1984 Apr;13(2):85-91

A clinicopathological study has been performed on a series of 42 well-documented examples of aneurysmal bone cyst of the jaws recorded in the literature, and 4 additional personally observed cases. Most occurred in the first three decades (93%), 2/3 of patients being younger than 20 years. There was a preponderance of females (62%). Read More

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Ascending ramus for reconstruction of the mandible.

Int J Oral Surg 1981 ;10(Suppl 1):42-6

We have developed a technique for an immediate bone graft utilizing the anterior part of the ascending ramus for repair of bone defects resulting from resection. We applied this operative procedure to a case of an extensive ossifying fibroma of the mandible. As a result, the postoperative x-ray examination showed a well-restored shape of the mandible, and the postoperative function was excellent. Read More

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September 1982