scholarly journals Benign Fibrous Histiocytoma of the Buccal Mucosa: Case Report and Literature Review

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Paraskevi Giovani ◽  
Anna Patrikidou ◽  
Aris Ntomouchtsis ◽  
Soultana Meditskou ◽  
Henri Thuau ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Head And Neck ◽  
Buccal Mucosa ◽  
Clinical Characteristics ◽  
Fibrous Histiocytoma ◽  
Relevant Literature ◽  
Benign Fibrous Histiocytoma ◽  
Neck Area

Benign fibrous histiocytoma is an interesting and challenging entity even in its most usual, cutaneous presentation. Noncutaneous presentation is extremely limited, even more so for the mucosa of the head and neck area. We herein report such a case, describing the clinical characteristics of the lesion, complete diagnostic evaluation, management, and follow-up. Diagnostic histopathological challenges are specifically illustrated. A complete review of the relevant literature is also included.

Clinical Correction of Complete Median Cleft of the Mandible and Lower Lip: A 17-Year Follow-Up of a Case Report With Literature Review

2021 ◽  
pp. 105566562199017
Author(s):  
Weidong Liu ◽  
Li Ma ◽  
Shizhou Zhang ◽  
Tengda Zhao
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Clinical Characteristics ◽  
Relevant Literature ◽  
Therapeutic Options ◽  
Lower Lip ◽  
Maxillofacial Development ◽  
Choice Of Treatment ◽  
Median Cleft

The median cleft of the mandible and lower lip is an extremely rare congenital maxillofacial deformity, and the therapeutic options are controversial. To evaluate the clinical characteristics and identify a better choice of treatment modes used among us and others, we reviewed 34 relevant literature and herein describe a 17-year follow-up of a case with a median cleft of the mandible and lower lip. Based on the literature and our case with good functional and aesthetical outcomes, we propose a prospective clinical treatment: Patients of Tessier 30 cleft associated with cleft of the mandible could undergo mandibular repair after puberty in conditions of a good occlusal relationship and normal maxillofacial development, even with mild masticatory dysfunction.

scholarly journals Multiple Clustered and Focally Atrophic Dermatofibromas: Case Report and Literature Review

2020 ◽  
Vol 7 (2) ◽  
pp. 1-3
Author(s):  
Gustavo Moreira Amorim ◽  
Eduardo Dan Itaya ◽  
Gabriela Coelho Itaya ◽  
Luiza Mousquer Leal ◽  
Amanda Amaro Pereira ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Fibrous Histiocytoma ◽  
Relevant Literature ◽  
Benign Fibrous Histiocytoma ◽  
Body Segment ◽  
Central Scar ◽  
Immunohistochemical Profile

We present a case of a 50 year-old woman with multiple erythematous and hyperpigmented plaques, with achromic and slightly atrophic centers, restricted to a body segment. Dermoscopy showed a pigmented network surrounding a central scar-like patch. Histopathology, complemented by immunohistochemical profile was compatible with dermatofibromas, arranged in a multiple clustered form. Relevant literature on the topic was reviewed. Meshterms: Factor 13a Positivity; Benign Fibrous Histiocytoma; Multiple clustered dermatofibroma; Segmental Distribution

Ameloblastic fibro-odontoma in a child patient: case report and literature review

2021 ◽  
Vol 10 (2) ◽  
pp. e26610212430
Author(s):  
Gustavo Zanna Ferreira ◽  
Carolina Ferrairo Danieletto-Zanna ◽  
Liogi Iwaki Filho ◽  
Rômulo Maciel Lustosa ◽  
Willian Pecin Jacomacci ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Bone Regeneration ◽  
Clinical Characteristics ◽  
Patient Case ◽  
Lesion Pattern ◽  
Local Bone ◽  
Ameloblastic Fibroma ◽  
Child Patient

The ameloblastic fibro-odontoma (AFO) is a mixed odontogenic tumor, with characteristics of ameloblastic fibroma, presenting enamel and dentin, which occurs more frequently in individuals aged 5 to 17 years. This paper reports na extensive case of ameloblastic fibro-odontoma in the mandible of a 3-year-old patient, discussed in comparison to cases selected from a brief literature review on the clinical characteristics, Evolution and therapeutic options for this lesion. In the last years, there was no consensus in the literature concerning its etiopathogenesis and classification, yet recently the AFO was classified as a developing odontoma. This case is in accordance with the 7 cases reported in the literature of AFO in the mandible of children aged 10 years or younger, especially concerning the lesion pattern and evolution and treatment adopted. The patient did not present relapse and exhibited local bone regeneration at the 3-year follow-up.

Benign fibrous histiocytoma of the buccal mucosa: Case report with immunohistochemical features

2003 ◽  
Vol 61 (2) ◽  
pp. 269-271 ◽  
Author(s):  
Fábio A. Alves ◽  
Pablo Agustin Vargas ◽  
Sheila Aparecida Coelho Siqueira ◽  
Ricardo D. Coletta ◽  
Oslei Paes de Almeida
Keyword(s):  
Case Report ◽  
Buccal Mucosa ◽  
Fibrous Histiocytoma ◽  
Benign Fibrous Histiocytoma

Another Cystic Lesion in the Calcaneus

2013 ◽  
Vol 103 (2) ◽  
pp. 141-144 ◽  
Author(s):  
Mert Keskinbora ◽  
Özkan Köse ◽  
Yildirim Karslioglu ◽  
Bahtiyar Demiralp ◽  
Mustafa Basbozkurt
Keyword(s):  
Differential Diagnosis ◽  
Male Patient ◽  
Bone Grafting ◽  
Cystic Lesion ◽  
Fibrous Histiocytoma ◽  
Relevant Literature ◽  
Long Bones ◽  
Cystic Lesions ◽  
Benign Fibrous Histiocytoma

Benign fibrous histiocytoma is a rare benign primary skeletal tumor that occurs frequently in the long bones and the pelvis. The calcaneus is an unusual location for benign fibrous histiocytoma. We did not identify any case of benign fibrous histiocytoma involving the calcaneus in the relevant literature. We describe a 22-year-old male patient with benign fibrous histiocytoma involving the calcaneus treated with curettage and bone grafting. At the final follow-up visit, 1 year after surgery, the patient was free of pain and walking unaided. We discuss the differential diagnosis of cystic lesions of the calcaneus. (J Am Podiatr Med Assoc 103(2): 141–144, 2013)

scholarly journals Benign Fibrous Histiocytoma: A Rare Case Report and Literature Review

2014 ◽  
Vol 15 (1) ◽  
pp. 116-120 ◽  
Author(s):  
D. Prasanna Kumar ◽  
Umesh ◽  
Tushar Rathi ◽  
Vaibhav Jain
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Fibrous Histiocytoma ◽  
Benign Fibrous Histiocytoma ◽  
Rare Case Report

scholarly journals Benign fibrous histiocytoma of the maxilla: A rare case report and literature review

2020 ◽  
Vol 11 (2) ◽  
pp. 298
Author(s):  
PrateekKumar Porwal ◽  
JitendraPratap Singh Chauhan ◽  
Abhay Kumar ◽  
RajeshKumar Thakur ◽  
Kailash Mittal ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Fibrous Histiocytoma ◽  
Benign Fibrous Histiocytoma ◽  
Rare Case Report

Intraspinal extradural benign fibrous histiocytoma of the lumbar spine in a pediatric patient. Case report and literature review

2016 ◽  
Vol 32 (8) ◽  
pp. 1549-1553 ◽  
Author(s):  
Fabrizio Donati ◽  
Luca Proietti ◽  
Aaron Burrofato ◽  
Domenico Alessandro Santagada ◽  
Francesco Ciro Tamburrelli
Keyword(s):  
Case Report ◽  
Lumbar Spine ◽  
Literature Review ◽  
Pediatric Patient ◽  
Fibrous Histiocytoma ◽  
Benign Fibrous Histiocytoma ◽  
Patient Case

scholarly journals Malignant Fibrous Histiocytoma Metastatic to the Thyroid Gland

2012 ◽  
Vol 3 (1) ◽  
pp. 30-32
Author(s):  
Akash Anand ◽  
Christina J Yang ◽  
Ronald G Amedee ◽  
Win Naing ◽  
Aynaud Foster Hebert
Keyword(s):  
Case Report ◽  
Thyroid Gland ◽  
Literature Review ◽  
Lower Extremity ◽  
Head And Neck ◽  
Malignant Fibrous Histiocytoma ◽  
Adjuvant Radiotherapy ◽  
Fibrous Histiocytoma ◽  
Disease Treatment ◽  
Case Basis

ABSTRACT Introduction Malignant fibrous histiocytoma (MFH) metastatic to the thyroid is rare. In this case report and literature review, we discuss the presentation, diagnosis and treatment of MFH. Materials and methods We present a case of MFH metastatic to the thyroid. A literature review on malignant fibrous histiocytoma involving the thyroid was performed. Results We present a case of MFH metastatic to the thyroid from a lower extremity primary, treated by excision. The initial diagnosis of MFH metastatic to the thyroid relies on history and histopathology. Treatment is excision, sometimes followed by adjuvant radiotherapy and/or chemotherapy. Conclusion This is the sixth documented case of MFH metastatic to the thyroid. Due to the rarity of this disease, treatment decisions should be made on a case-by-case basis. How to cite this article Yang CJ, Anand A, Amedee RG, Naing W, Hebert AF. Malignant Fibrous Histiocytoma Metastatic to the Thyroid Gland. Int J Head and Neck Surg 2012;3(1): 30-32.

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