scholarly journals Clinicopathological, histochemical and immunohistochemical aspects of angioleiomyoma of the cheek: a case report

2016 ◽  
Vol 31 (2) ◽  
pp. 101
Author(s):  
Paula Daniele Matheus ◽  
Manoela Domingues Martins ◽  
Luise Meurer ◽  
Lucas N. Sant´Ana ◽  
Manoel Santa’Ana Filho
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Gastrointestinal Tract ◽  
Oral Cavity ◽  
Buccal Mucosa ◽  
Immunohistochemical Analysis ◽  
Surgical Excision ◽  
Left Cheek ◽  
Local Surgical Excision ◽  
Epithelioid Leiomyoma

Introduction: Leiomyomas are benign smooth muscle neoplasms that preferably affect the genitals, skin, and gastrointestinal tract, being rarely seen in the oral cavity. They  re commonly classified into three microscopic patterns: solid leiomyoma, angioleiomyoma (ALM), and epithelioid leiomyoma. The most frequently reported sites of occurrence of oral ALM are the lip (48.6%), palate (21.1%), buccal mucosa and tongue (9.2%), and intraosseous lesions (8.3%).Case report: A 62 years old male presented a painless swelling in the left cheek. In this report histopathological and immunohistochemical analysis were made to confirm the diagnosis, since several lesions were possible. The treatment was local surgical excision of the tumor.

Epidermoid Cyst of the Buccal Mucosa: A Case Report

2007 ◽  
Vol 8 (3) ◽  
pp. 90-96 ◽  
Author(s):  
Fatih Ozan ◽  
Hidayet Burak Polat ◽  
Sinan Ay ◽  
Fahrettin Goze
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Buccal Mucosa ◽  
Epidermoid Cyst ◽  
Rare Case ◽  
Neck Region ◽  
Facial Asymmetry ◽  
Left Cheek ◽  
Review Of The Literature ◽  
Head And Neck Region

Abstract Aim The purpose of this article is to describe a rare case of an epidermoid cyst in the buccal cheek region and a review of the literature. Background Dermoid and epidermoid cysts are developmental pathologies occurring in the head and neck region with an incidence ranging from 1.6% to 6.9%, and both cysts reported in less than 0.01% of all oral cavity cysts. Report A rare case of an epidermoid cyst originating from the buccal mucosa in a 38-year-old woman with a complaint of swelling and facial asymmetry in the left cheek just distal to the commissure for six months is presented in this report. Citation Ozan F, Polat HB, Ay S, Goze F. Epidermoid Cyst of the Buccal Mucosa: A Case Report. J Contemp Dent Pract 2007 March;(8)3:090-096.

scholarly journals Multiple Oral Leiomyomas in an Infant: A Rare Case

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Efraín Alvarez ◽  
María P. Laberry ◽  
Carlos M. Ardila
Keyword(s):  
Smooth Muscle ◽  
Gastrointestinal Tract ◽  
Oral Cavity ◽  
Rare Case ◽  
Surgical Excision ◽  
Smooth Muscle Tumor ◽  
Review Of The Literature ◽  
Histological Studies ◽  
Floor Of The Mouth ◽  
Muscle Tumor

Oral leiomyoma is a benign smooth muscle tumor that occurs most frequently in the uterine myometrium, gastrointestinal tract, and skin. Incidence in the oral cavity is considered uncommon. Most cases are reported in adults, with very few cases described in children. A rare case of multiple leiomyomas localized on the tongue, cheek, and floor of the mouth of an 8-month-old baby is reported. The diagnosis of leiomyoma in the oral cavity is mainly determined by histological studies; however, immunohistochemical tests are recommended in order to differentiate from other tumors. Surgical excision of the lesion appears to be the best treatment option. A review of the literature did not reveal any previously reported case of multiple oral leiomyomas.

scholarly journals Cellular Angiofibroma of the Buccal Mucosa: A Rare Case Report and Review of Literature

2012 ◽  
Vol 1 (1) ◽  
pp. 23-25
Author(s):  
Kamran Bokhari ◽  
Luqman Manikandan ◽  
Ajmal Mohammad ◽  
Mohammad Shahul ◽  
Mustafa Abdul Bagi ◽  
...  
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Soft Tissues ◽  
Surgical Excision ◽  
Histopathological Diagnosis ◽  
Review Of Literature ◽  
Cellular Angiofibroma ◽  
Rare Case Report

ABSTRACT Background Cellular angiofibromas are rare benign mesenchymal neoplasms characterized by spindle cell component and numerous small vessels. They are commonly well-circumscribed, localized in the superficial soft tissues. The lesion is more frequently seen in the inguinoscrotal or vulvovaginal regions and occurs equally in men and women, and rarely involves oral cavity. Due to its clinical and histological similarity with other mesenchymal tumors, such as angiomyoma, hemangioma, lymphangioma and hemangiopericytoma, angiofibroma presents a diagnostic dilemma. Case report Very few cases of angiofibroma involving maxillofacial region have been reported in the literature. This case report involves cellular angiofibroma involving left buccal mucosa in a 23-year-old female patient. Following detailed clinical examination, radiological interpretation and histopathological diagnosis, surgical excision was performed. The patient was followed-up on a regular basis and was disease free. Summary and conclusion Benign angiofibroma involving oral cavity is a rare tumor. There is a close resemblance of this tumor with other mesenchymal lesions and, thus, faces a diagnostic challenge. Surgical excision with a long-term followup gives good prognosis to this lesion—benign cellular angiofibroma. How to cite this article Bokhari K, Manikandan L, Mohammad A, Shahul M, Bagi MA, Kota Z. Cellular Angiofibroma of the Buccal Mucosa: A Rare Case Report and Review of Literature. Int J Exper Dent Sci 2012;1(1):23-25.

scholarly journals Acquired smooth muscle hamartoma: A case report on the lower extremity with hidrosis

2019 ◽  
Vol 7 ◽  
pp. 2050313X1989383
Author(s):  
Malika A Ladha ◽  
Todd Remington
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Lower Extremity ◽  
Smooth Muscle Cells ◽  
English Literature ◽  
Surgical Excision ◽  
Muscle Cells ◽  
Clinical Spectrum ◽  
Rare Entity ◽  
First Case

Smooth muscle hamartomas are benign dermal proliferations of smooth muscle cells. Smooth muscle hamartomas are sub-divided into congenital or acquired; the latter is a rare entity with less than 20 cases being reported in the English literature. Most often asymptomatic, acquired smooth muscle hamartomas follow an indolent course. Treatment in the form of surgical excision can be utilized for symptomatic or cosmetic purposes. Here, we report the first case of an acquired smooth muscle hamartomas of the shin which also uniquely presented with hidrosis. This case highlights the varied clinical spectrum of acquired smooth muscle hamartomas.

scholarly journals Angioleiomyoma of the Larynx: A Case Report and Literature Review

2020 ◽  
Vol 99 (10) ◽  
pp. 658-663
Author(s):  
Federica Perardi ◽  
Giuseppe Abbate ◽  
Leonardo R. Iannuzzelli ◽  
Rossella Contini ◽  
Manuela De Munari ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Differential Diagnosis ◽  
Smooth Muscle ◽  
Case Report ◽  
Gold Standard ◽  
Carbon Dioxide Laser ◽  
Standard Treatment ◽  
Surgical Excision ◽  
Laser Technology ◽  
Complete Surgical Excision

Angioleiomyoma is a benign smooth muscle and vessel tumor; laryngeal localization is extremely rare with only 24 cases described in the literature; moreover, it should be considered in the differential diagnosis of laryngeal mass. Endoscopic complete surgical excision with dissection along capsule is now considered the gold-standard treatment for small and well-circumscribed laryngeal angioleiomyoma. We present a case of laryngeal angioleiomyoma successfully treated with carbon dioxide laser technology which resulted in a bleeding reduction and adequate hemostasis with less tissue damage and good functional outcome.

scholarly journals Pyogenic granuloma - report of three cases in rare sites

2013 ◽  
Vol 12 (4) ◽  
pp. 445-448
Author(s):  
AN Sulabha ◽  
S Choudhari ◽  
G Suchitra
Keyword(s):  
Oral Cavity ◽  
Buccal Mucosa ◽  
Hard Palate ◽  
Medical Science ◽  
Surgical Excision ◽  
Pyogenic Granuloma ◽  
Patient Treatment ◽  
Young Females ◽  
One Year

Pyogenic granuloma is a benign, localized mass of exuberant granulation tissue produced in response to various stimuli. It is inflammatory hyperplasia of oral cavity commonly seen on gingival area and rarely on other parts of oral cavity such as lips, tongue, palate and buccal mucosa. It is seen predominantly in 2nd to 3rd decade of life in young females. Clinically manifesting as small red erythematous exophytic lesion, it must be biopsied to rule out other serious conditions. This article aims to present three cases of extra gingival pyogenic granulomas occurring in rare sites such as buccal mucosa, anterior hard palate and alveolar mucosa of completely edentulous ridge in maxilla. Pyogenic granuloma on buccal mucosa and anterior hard palate were seen in female patients with age of 40 years and 34 years respectively and pyogenic granuloma on alveolar mucosa of edentulous ridge in maxilla was noted in 70 years old male patient. Surgical excision was performed for all the lesion and follow up of one year did not show any recurrence. Please add little description of patient + treatment + followup results. DOI: http://dx.doi.org/10.3329/bjms.v12i4.16667 Bangladesh Journal of Medical Science Vol. 12 No. 04 October ’13 Page 445-448

scholarly journals Mucocele of the glands of blandin nuhn: a case report

2013 ◽  
pp. 46-47 ◽  
Author(s):  
Nathalia García-León ◽  
Gilberto E Marrugo
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Clinical Presentation ◽  
Surgical Excision ◽  
Diagnosis And Treatment ◽  
Vascular Lesions ◽  
Benign Lesions ◽  
Recurrent Lesion ◽  
Timely Diagnosis

Mucoceles arising from the Blandin Nuhn glands are uncommon benign lesions of the oral cavity, which by their clinical presentation may be confused with more serious diseases such as vascular lesions, pyogenic granulomas, polyps, or squamous papillomas; thereby, it is convenient to be aware of the characteristics of this entity to guide the accurate and timely diagnosis and treatment. Herein, we present a case of a 10-year-old patient with a recurrent lesion of this type, which required surgical excision and marsupialization of the same, with no evidence of recurrence during follow-up.

scholarly journals The Treatment of Lymphangioma in the Buccal Mucosa by Surgical Excision: A Rare Case Report

2018 ◽  
Vol 2 (1) ◽  
Author(s):  
Lacin Nihat ◽  
Yalcin Mustafa ◽  
Efeoglu Bayram Fatih ◽  
Izol Bozan Serhat ◽  
Tünel Aynur
Keyword(s):  
Case Report ◽  
Buccal Mucosa ◽  
Rare Case ◽  
Surgical Excision ◽  
Rare Case Report

scholarly journals Epidermoid Cyst of the Buccal Mucosa: An Uncommon Entity. Case report and literature review

2021 ◽  
Author(s):  
nouha dammak ◽  
abdellatif chokri ◽  
afef slim ◽  
Ahlem Bellalah ◽  
Adel Bouguezzi ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Cavity ◽  
Buccal Mucosa ◽  
Epidermoid Cyst ◽  
The Body ◽  
Benign Lesions

Epidermoid, dermoid and teratoid cysts are nonodontogenic benign lesions derived from the germinative epithelium, appearing any where of the body. In the oral cavity, these are uncommon and account for less than 0.01% of all the oral cysts. These cysts often remain asymptomatic for years however can become acutely symptomatic.

scholarly journals MULTIPLE HEMANGIOMATOSE DISEASE INVOLVING GASTROINTESTINAL TRACT: A CASE REPORT.

2020 ◽  
Vol 7 (1) ◽  
pp. 55-58
Author(s):  
Clara Leticia Rocha Silva ◽  
Julia Artiaga de Carvalho Coelho ◽  
Isabella Vilane Braga Saboia Rythowem ◽  
Pedro Miranda Portugal Junior ◽  
Heloyse Nascimento Lima ◽  
...  
Keyword(s):  
Case Report ◽  
Gastrointestinal Tract ◽  
Oral Cavity ◽  
General Public ◽  
Public Hospital ◽  
Vascular Tumor ◽  
Ear Canal ◽  
Digestive Hemorrhage ◽  
Colon And Rectum

Hemangiomas are a type of benign vascular tumor, originated from angiogenesis disorders and prevalent in approximately 4% to 5% of the population. Among the most common complications are: ulcerations and bleeding, in cases of those located in the gastrointestinal tract; impairment of airways and vision; visceral complications; obstruction of the ear canal causing deficit in hearing; or problems in eating or in the emission of sounds due to its presence in the oral cavity. Colon and rectum hemangiomas are a rare cause of lower digestive hemorrhage. The aim of this study is to demonstrate the case of multiple hemangiomatose disease in an inpatient undergoing treatment at the Palmas General Public Hospital (HGPP).

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