scholarly journals Prenatal Diagnosis of Congenital Mesenchymal Hamartoma of Liver: A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Sreelakshmi Kodandapani ◽  
Muralidhar V. Pai ◽  
Vijay Kumar ◽  
Kanthilatha V. Pai
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Unusual Case ◽  
Benign Tumor ◽  
Mesenchymal Hamartoma ◽  
Rare Benign Tumor ◽  
Abdominal Cyst

Hepatic mesenchymal hamartoma is a rare benign tumor. We present an unusual case of a fetal abdominal cyst, later diagnosed histopathologically to be mesenchymal hamartoma of liver. The organ of origin was indeterminate on both prenatal and postnatal ultrasounds. As there are no specific sonological findings, whenever a large multicystic fetal abdominal cyst is seen, mesenchymal hamartoma should be considered as a possibility.

scholarly journals Dentofacial Deformity Caused by Bulky Osteochondroma: Report of an Unusual Case and the Importance of Cone Beam Computed Tomography

2017 ◽  
Vol 11 (1) ◽  
pp. 237-241 ◽  
Author(s):  
Weeraya Tantanapornkul ◽  
Kittipong Dhanuthai ◽  
Phonkit Sinpitaksakul ◽  
Chumpot Itthichaisri ◽  
Paksinee Kamolratanakul ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Differential Diagnosis ◽  
Case Report ◽  
Unusual Case ◽  
Benign Tumor ◽  
Mandibular Condyle ◽  
Cone Beam ◽  
Dentofacial Deformity ◽  
Alternative Modality ◽  
Rare Benign Tumor

Introduction: Osteochondroma of mandibular condyle is a rare benign tumor. Case Report: This case report described clinical, radiographic features, differential diagnosis, histopathologic correlation and treatment of condylar osteochondroma. Conclusion: Conebeam computed tomography (CBCT) is an alternative modality to CT or MRI that should be performed in all cases of suspected osteochondroma of the mandibular condyle.

An Invasive Hemolymphangioma of the Pancreas in a Young Woman

2019 ◽  
Vol 21 (10) ◽  
pp. 798-800 ◽  
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

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.

scholarly journals Leiomyoma: a case report of a rare benign tumor of the female urethra

2015 ◽  
Vol 22 ◽  
Author(s):  
Amine Slaoui ◽  
Abdelouahed Lasri ◽  
Tarik Karmouni ◽  
Khalid Elkhader ◽  
Abdelatif Koutani ◽  
...  
Keyword(s):  
Case Report ◽  
Benign Tumor ◽  
Female Urethra ◽  
Rare Benign Tumor

scholarly journals Laparoscopic Resection of a Giant Dedifferentiated Primary Retroperitoneal Mucinous Cystadenoma (PRMC) in a Young Woman: A Case Report and Literature Review

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Wu L ◽  
Li X ◽  
Li J ◽  
Lai Y
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Benign Tumor ◽  
Laparoscopic Resection ◽  
Abdominal Cavity ◽  
Mucinous Cystadenoma ◽  
Rare Benign Tumor ◽  
Primary Retroperitoneal

Background: PRMC is a very rare benign tumor of the abdominal cavity that usually occurs in women, and PRMC demonstrate no specific findings on CT. There are many reports on the differential diagnosis and discussion of PRMC imaging, but there are few reports on the treatment of dedifferentiated PRMC using laparoscopic resection and postoperative follow-up.

scholarly journals Cervical Hibernoma, a Rare, Benign Tumor: Case Report

2011 ◽  
Vol 90 (1) ◽  
pp. E19-E21 ◽  
Author(s):  
Brandon L. Prendes ◽  
Chitra Kohli ◽  
John S.J. Brooks ◽  
Jason G. Newman
Keyword(s):  
Case Report ◽  
Benign Tumor ◽  
Rare Benign Tumor

Clinical Presentation and Anatopathologic Finding of a Hepatic Vascular Hamartoma: a Case Report.

2018 ◽  
Vol 17 (5) ◽  
pp. 0-10
Author(s):  
Valentina Ferri ◽  
Benedetto Ielpo ◽  
Hipolito Duran ◽  
Eduardo Diaz ◽  
Isabel Fabra ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Benign Tumor ◽  
Vascular Tissue ◽  
Clinical Presentation ◽  
Mesenchymal Hamartoma ◽  
Total Excision ◽  
Pathologic Findings ◽  
Vascular Hamartoma

HVH (hepatic vascular hamartoma) is a tumor like malformation arising from the vascular tissue of the liver. HVH has been previously reported in animals and presents distintive features from the most frequent benign tumor like malformation of the liver, the hepatic mesenchymal hamartoma (HMH). Herein we report a case of HVH localized in hepatic segment 4b, involving the gastro hepatic ligament, successfully treated with total excision. We describe the anatomo-pathologic findings focusing on the clinical and radiological presentation, the intraoperative characteristics and the differential diagnosis.

scholarly journals Odontogenic Myxoma of the Maxilla - A Case Report

2019 ◽  
Vol 6 ◽  
Author(s):  
Adil Eabdenbtsen ◽  
Mohammed Mouzouri ◽  
Ahlam Bellouchi ◽  
Noureddine Oulali ◽  
Mohammed Bouziane ◽  
...  
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Benign Tumor ◽  
High Rate ◽  
Odontogenic Myxoma ◽  
Radical Treatment ◽  
Rare Benign Tumor ◽  
The Right

Introduction : The odontogenic myxoma is a rare benign tumor of the maxilla, whose clinical and radiological manifestations are variable and nonspecific and can be confused with other radiolucent lesions. Its origin would be the embryonic mesenchyme of the dental follicle.Case report : We report the case of odontogenic myxoma of the right maxilla, discovered by chance in a 25 year old patient. Clinically, the patient had painless, firm on palpation, swelling of the right maxilla, impeding chewing and speech. Facial CT-scan showed an expansive osteolytic process blowing the right maxilla off. A biopsy was in favor of an odontogenic myxoma. The diagnosis was based on clinical, radiological and especially anatomopathological arguments.Conclusion : The local aggressiveness of the odontogenic myxoma and its high rate of recurrence justify a radical treatment beyond the lesion’s boundaries and thus imply a postoperative repair.

scholarly journals INTRA-ARTICULAR SYNOVIAL HEMANGIOMA OF KNEE OVERLYING POSTERIOR CRUCIATE LIGAMENT - A CASE REPORT

2012 ◽  
Vol 02 (03) ◽  
pp. 42-44
Author(s):  
Dileep K. S. ◽  
Sandeep V. Kanakaraddi ◽  
Vidyasagar J.V. S. ◽  
Radha S. ◽  
Akshatha Rao Aroor
Keyword(s):  
Case Report ◽  
Knee Joint ◽  
Posterior Cruciate Ligament ◽  
Benign Tumor ◽  
Cruciate Ligament ◽  
Signs And Symptoms ◽  
Mri Findings ◽  
Synovial Hemangioma ◽  
Rare Benign Tumor

AbstractHemangioma of synovium is a rare benign tumor that can arise from any surface lined by synovium. Intra-articular synovial hemangioma is most common in the knee joint. The diagnosis is difficult as the signs and symptoms are nonspecific. We hereby report a hitherto unreported case of synovial hemangioma of knee overlying posterior cruciate ligament, its MRI findings and discuss the appropriate management

Parapharyngeal Ganglioneuroma with Neurofibromatosis: An Unusual Presentation

2011 ◽  
Vol 120 (12) ◽  
pp. 769-774 ◽  
Author(s):  
Parul Sinha ◽  
Suresh C. Sharma ◽  
Shipra Agarwal ◽  
Siddhartha Datta Gupta
Keyword(s):  
Unusual Case ◽  
Benign Tumor ◽  
Parapharyngeal Space ◽  
Treatment Approach ◽  
Hypertensive Crisis ◽  
Neurogenic Tumors ◽  
Appropriate Treatment ◽  
Rare Benign Tumor ◽  
Hypertensive Crises ◽  
Biochemical Features

Objectives: Ganglioneuroma is a rare benign tumor of the sympathetic nervous system that is seldom localized to the head and neck. Rarer still are cases of functional ganglioneuroma with catecholamine production. We report an unusual case of a large parapharyngeal space ganglioneuroma in a patient with neurofibromatosis that caused an intraoperative hypertensive crisis in the absence of a neuroblastomatous component — Hitherto an undocumented complication. Methods: We present a case of functional parapharyngeal ganglioneuroma and review the clinicopathologic and biochemical features of these rare tumors. Results: Fewer than 40 anecdotal cases of parapharyngeal ganglioneuromas have been reported, and there is a lack of ade quate literature on the biology and appropriate treatment approach of these tumors. Conclusions: Our case illustrates the importance of vigilant preoperative precautions in the management of neurogenic tumors, particularly ganglioneuromas. These usually nonfunctional tumors can result in sudden intraoperative and postoperative hypertensive crises even in the absence of any preoperative autonomic symptoms.

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