Desmoplastic Trichoepithelioma: An Unusual Location

Desmoplastic trichoepithelioma is a rare benign tumor emerging from the hair follicle. Here, we report an unusual nasal location of a desmoplastic trichoepithelioma in a female patient

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Odontogenic myxofibroma- Report of a rare entity

Journal of Pathology of Nepal ◽

10.3126/jpn.v6i12.16262 ◽

2016 ◽

Vol 6 (12) ◽

pp. 1043-1045

Author(s):

P Poudel ◽

B Bajracharya ◽

S Bhattacharya ◽

D Bajracharya ◽

S Singh ◽

...

Keyword(s):

Female Patient ◽

Recurrence Rate ◽

Rare Case ◽

Benign Tumor ◽

Final Diagnosis ◽

High Recurrence Rate ◽

Rare Entity ◽

Odontogenic Myxoma ◽

Immunohistochemical Examination ◽

Rare Benign Tumor

Odontogenic myxofibroma is a rare, benign tumor, which is considered to be the variant of odontogenic myxoma. It is locally infiltrative, aggressive and has high recurrence rate. Only 24 specific cases of myxofibroma have been reported since 1950 and only two cases have been reported with excessive calcifications till 2012. Here, we report a rare case of Odontogenic myxofibroma with calcifications in 53 years old female patient who presented with the chief complain of swelling. The final diagnosis of Odontogenic myxofibroma was established after histopathological and immunohistochemical examination.

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Intramuscular Hemangioma in Lip Treated with Sclerotherapy and Surgery

Case Reports in Dentistry ◽

10.1155/2011/302451 ◽

2011 ◽

Vol 2011 ◽

pp. 1-4 ◽

Cited By ~ 2

Author(s):

Vanessa A. Silva ◽

Nádia L. Lima ◽

Ana Terezinha M. Mesquita ◽

Esmeralda Maria da Silveira ◽

Flaviana D. Verli ◽

...

Keyword(s):

Female Patient ◽

Benign Tumor ◽

Upper Lip ◽

Rare Benign Tumor ◽

Vascular Origin ◽

Intramuscular Hemangioma

Intramuscular hemangioma is a relatively rare, benign tumor of vascular origin, accounting for less than 1% of all hemangiomas. This paper reports a case of a 48-year-old female patient with intramuscular hemangioma in the upper lip, treated with sclerotherapy and subsequent complementary surgery.

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Osteoblastoma of the rib: A rare benign tumor with an unusual location

International Journal of Surgery Case Reports ◽

10.1016/j.ijscr.2012.09.016 ◽

2013 ◽

Vol 4 (2) ◽

pp. 146-148 ◽

Cited By ~ 1

Author(s):

Stamatis Katsenos ◽

Stavros Archondakis ◽

Timotheos Sakellaridis

Keyword(s):

Benign Tumor ◽

Unusual Location ◽

Rare Benign Tumor

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Case for diagnosis

Anais Brasileiros de Dermatologia ◽

10.1590/abd1806-4841.20132515 ◽

2013 ◽

Vol 88 (6) ◽

pp. 997-999 ◽

Cited By ~ 1

Author(s):

Joanna Pimenta de Araujo Franco ◽

Luciana Helena Zacaron ◽

Ricardo Barbosa Lima ◽

Antônio Macedo D'Acri ◽

Carlos José Martins

Keyword(s):

Surgical Treatment ◽

Head And Neck ◽

Female Patient ◽

Benign Tumor ◽

Middle Aged ◽

Excellent Outcome ◽

Subcutaneous Nodules ◽

Chondroid Syringoma ◽

Cutaneous Tumor ◽

Rare Benign Tumor

The chondroid syringoma is a rare benign tumor, also called mixed cutaneous tumor by the presence of epithelial and mesenchymal components, consisting of sweat elements in cartilaginous, collagenous, myxoid or osseous stroma, among others. It mainly affects middle-aged men and is characterized by asymptomatic and slowgrowing, dermal or subcutaneous nodules. The most common locations are the head and neck. It is rare on the extremities. There are reports of malignant variants predominantly in women, located on the extremities. We report a case of a female patient with a lesion on the toe, with excellent outcome after surgical treatment.

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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.

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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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Management of Basal Cell Adenoma of Accessory Parotid Gland Through Transoral Approach: Report of a Rare Case With Review

Craniomaxillofacial Trauma & Reconstruction Open ◽

10.1177/24727512211030839 ◽

2021 ◽

Vol 6 ◽

pp. 247275122110308

Author(s):

Charudatta Naik ◽

Sanjay Joshi ◽

Bhupendra Mhatre ◽

Sneha Punamiya

Keyword(s):

Parotid Gland ◽

Basal Cell ◽

Benign Tumor ◽

Transoral Approach ◽

Surgical Approaches ◽

Basal Cell Adenoma ◽

Diagnostic Dilemma ◽

Cell Adenoma ◽

Rare Benign Tumor ◽

Accessory Parotid Gland

Diagnosis of mid-cheek mass has always been a diagnostic dilemma for clinicians. The incidence of the accessory parotid gland (APG) has been well documented in the literature. However, a diverse spectrum of pathologies can arise from this accessory parotid tissue. Basal cell adenoma is a rare benign tumor that predominantly affects the parotid gland. Its occurrence in the accessory parotid gland has been documented in 9 cases till date. Surgical approaches for the management of such APG lesions have been in debate. This report documents a case of Basal Cell Adenoma arising in accessory parotid tissue in a 55-year-old woman who was treated by transoral excision. This paper also reviews previously documented cases of all APG lesions and attempts to elucidate the rationale for selecting an appropriate surgical approach.

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Robotic, totally endoscopic excision of mitral valve papillary fibroelastoma

10.1510/mmcts.2021.045 ◽

2021 ◽

Keyword(s):

Mitral Valve ◽

Aortic Valve ◽

Tricuspid Valve ◽

Benign Tumor ◽

Pulmonary Valve ◽

Papillary Fibroelastoma ◽

Robotic Assisted ◽

Endoscopic Excision ◽

Rare Benign Tumor ◽

Sixth Decade

Papillary fibroelastoma is a rare, benign tumor that affects males more frequently than females and that tends to be diagnosed during the fifth or sixth decade of life. It tends to arise on cardiac valves, with the aortic valve being the most frequent location followed by the mitral valve, the tricuspid valve, and the pulmonary valve. We present the case of a robotic-assisted, totally endoscopic excision of a mitral valve papillary fibroelastoma.

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