Capillary hemangioma as a rare benign tumor of the oral cavity: a case report

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.

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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.

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

Pan African Medical Journal ◽

10.11604/pamj.2015.22.111.7785 ◽

2015 ◽

Vol 22 ◽

Cited By ~ 1

Author(s):

Amine Slaoui ◽

Abdelouahed Lasri ◽

Tarik Karmouni ◽

Khalid Elkhader ◽

Abdelatif Koutani ◽

...

Keyword(s):

Case Report ◽

Benign Tumor ◽

Female Urethra ◽

Rare Benign Tumor

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

Journal of Clinical Case Studies ◽

10.16966/2471-4925.215 ◽

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.

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Cervical Hibernoma, a Rare, Benign Tumor: Case Report

Ear Nose & Throat Journal ◽

10.1177/014556131109000116 ◽

2011 ◽

Vol 90 (1) ◽

pp. E19-E21 ◽

Cited By ~ 1

Author(s):

Brandon L. Prendes ◽

Chitra Kohli ◽

John S.J. Brooks ◽

Jason G. Newman

Keyword(s):

Case Report ◽

Benign Tumor ◽

Rare Benign Tumor

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Atypical Presentation of Capillary Hemangioma in Oral Cavity- A Case Report

JOURNAL FOR CLINICAL AND DIAGNOSTIC RESEARCH ◽

10.7860/jcdr/2015/14276.6691 ◽

2015 ◽

Cited By ~ 1

Author(s):

Veena Raj Vasantha Kumari

Keyword(s):

Case Report ◽

Oral Cavity ◽

Capillary Hemangioma ◽

Atypical Presentation

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

Case Reports in Obstetrics and Gynecology ◽

10.1155/2011/932583 ◽

2011 ◽

Vol 2011 ◽

pp. 1-3 ◽

Cited By ~ 2

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.

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Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection

Journal of Neurological Surgery Reports ◽

10.1055/s-0037-1600913 ◽

2017 ◽

Vol 78 (01) ◽

pp. e52-e54

Author(s):

Dalila Forte ◽

Amets Irañeta ◽

Anabela Nabais ◽

António Figueiredo ◽

Manuela Mafra ◽

...

Keyword(s):

Clinical Case ◽

Benign Tumor ◽

Rare Complication ◽

Traumatic Injury ◽

Neck Region ◽

Capillary Hemangioma ◽

Nasal Packing ◽

Pathological Examination ◽

Lobular Capillary Hemangioma ◽

Rare Benign Tumor

Background Lobular capillary hemangioma is a rare benign tumor, most frequently located in the head or neck region, the nasal cavity being uncommonly affected. Its etiopathogenesis is not fully established, although traumatic and hormonal factors have been implied. Case Description A 50-year-old female patient underwent an uneventful endoscopic transsphenoidal removal of a pituitary cystic macroadenoma at our institution. Nasal packing was used in postoperative hemostasis. Histopathology was compatible with a gonadotrophin-producing adenoma. One month after the surgery, the patient presented with frequent episodes of epistaxis and a progressively growing nasal mass, which was removed endoscopically. Its pathological examination confirmed a lobular capillary hemangioma. Conclusions The authors present a clinical case combining two possible predisposing factors to the development of a nasal lobular capillary hemangioma: local traumatic injury through surgery and postoperative nasal packing and hormonal influence. This lesion is a rare complication of endoscopic transsphenoidal resections of pituitary adenomas.

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Recurrent endobronchial fibro-epithelial polyposis in a 73-year-old woman

Immunopathologia Persa ◽

10.34172/ipp.2021.14 ◽

2021 ◽

Vol 7 (2) ◽

pp. e14-e14

Author(s):

Ramin Sami ◽

Mina Nickpour ◽

Noushin Afshar Moghaddam

Keyword(s):

Case Report ◽

Oral Cavity ◽

Rare Case ◽

Benign Tumor ◽

Main Bronchus ◽

Rare Condition ◽

Genitourinary Tract ◽

Fibroepithelial Polyp ◽

Interventional Bronchoscopy ◽

Case Presentation

Introduction: Fibroepithelial polyp (FEP) is a benign tumor that is presented frequently in some of the organs like oral cavity, skin, colon and genitourinary tract, but in airway is rare. Case Presentation: We present a rare case in this paper, with recurrent bronchial FEP that was near completely obstructed right main bronchus that we managed her successfully with interventional bronchoscopy. In this case report we describe this rare condition. Conclusion: Airway FEP is uncommon benign tumor that may obstruct airways and rarely may be recurrent like our case.

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