scholarly journals Fibrous Histiocytoma of Anterior Ethmoidal Sinus: Case Report and Review of the Literature

2021 ◽  
pp. 1304-1309
Author(s):  
Mohammad Sharifi ◽  
Bahar Tafaghodi Yousefi

Benign fibrous histiocytoma of the para nasal sinus is a rare tumor of this region which originates from mesenchymal cells. A 9-year-old girl presented with gradually enlarging mass above the medial canthus over 3 months. Orbital computerized tomography scan showed a round well-differentiated homogeneous mass in the anterior ethmoidal sinus. Histology and immunohistochemistry analysis after excision revealed proliferation of spindle-shaped fibroblasts in storiform pattern and histiocytes without mitosis and anaplasia. After 9 months from surgical excision, recurrence occurred which resulted in total excision again. This is the first reported case of benign fibrous histiocytoma involving the ethmoid sinus in Iranian people. Rare sinus tumor should be considered in the differential diagnosis of sinus tumors.

2003 ◽  
Vol 4 (2) ◽  
pp. 74-79 ◽  
Author(s):  
Ümit Ertaş ◽  
M. Cemil Büyükkurt ◽  
Yasin Çiçek

Abstract Benign fibrous histiocytoma is a rare and usually painless oral neoplasm found in adults that may affect either soft tissue or bone typically noted in their fifth decade. This case was found in a 32 year-old Caucasian male who presented with a fairly well circumscribed unilocular radiolucent lesion extending from the mandibular right first incisor to the left first premolar and reaching the inferior mandible on a panoramic radiograph. A bony window was created and the intrabony lesion was curetted. Multiple sections revealed a cellular tumor composed of uniform spindle-shaped cells arranged in a prominent whorled or storiform pattern. Scattered xanthoma cells, multinucleated giant cells, lymphocytes, and deposits of hemosiderin were noted throughout the lesional stroma. Although malignant fibrous histiocytoma of the bone is relatively well known, benign fibrous histiocytoma of the bone is very rare. Citation Ertas U, Büyükkurt MC. Benign Fibrous Histiocytoma: Report of Case. J Contemp Dent Pract 2003 May;(4)2:074-079.


2021 ◽  
Vol 9 (C) ◽  
pp. 198-203
Author(s):  
Andi Hardianty ◽  
Khairuddin Djawad ◽  
Siswanto Wahab ◽  
Airin Nurdin

BACKGROUND: Dermatofibroma (DF) is a common benign skin tumor (Benign Fibrous Histiocytoma) that mostly affects the extremities with a tendency to occur more often in older females than males. It usually presents as a slow growing small brown dome shape papule on the extremities. DF has a chronic nature and can sometimes regresses spontaneously. Dermoscopy is essential in the evaluation of DF to help differentiate it with other skin tumors. The gold standard evaluation for diagnosis of DF is biopsy with histopathologic examination. Removal of DF is often due to cosmetic factors, with surgical excision being the preferred method for removal. DF has an excellent prognosis. CASE REPORT: We present two case reports of women with hyperpigmented nodules on the lower extremity. Dimple sign was positive. From dermoscopic study showed a pigment network and central white patch pattern. On histologic examination revealed proliferation of fibroblast such as spindle cells as a storiform pattern and hyperplastic epidermis with hyperpigmentation of the basal layer. Based on clinical features, dermoscopy and histopathological evaluation, the diagnosis of DF was established. Both patients were perform surgically excision and have a good result. CONCLUSION: Dermatofibroma is benign fibrous histiocytoma that represents one of the most common skin tumours. Nodular hyperpigmented dermatofibroma is a clinical variant of Dermatofibroma which can be treated with surgical excision with good prognosis.


2020 ◽  
Author(s):  
Tianming Yang ◽  
Lin Xiao ◽  
Huijun Ren

Abstract Background: Liposarcoma is common in adults. However, its occurrence in the retropharyngeal space is extremely rare, and no cases of liposarcoma in the prevertebral space have been reported before.Case presentation: A 78-year-old man presented to the Otolaryngology Department with a 1-year history of progressive dysphagia and a 1-month history of dyspnea and dysphonia. A computed tomography scan of his neck demonstrated a large retropharyngeal mass. Magnetic resonance imaging was performed to further characterize this mass. Based on the above examinations, retropharyngeal liposarcoma was first made. The patient underwent transoral surgical excision with the help of nasal endoscope. During surgery, the tumor was found to lie in the prevertebral space. Combine with histological examination, the diagnosis was modified to liposarcoma of the prevertebral space. Conclusions: It’s difficult to distinguish the enormous retropharyngeal tumors and prevertebral tumors using imaging. Complete excision via transoral approach maybe enough for these tumors.


2007 ◽  
Vol 23 (1) ◽  
pp. 73-75 ◽  
Author(s):  
Sharon R. Morris ◽  
Jean-Louis DeSousa ◽  
Andrew W. Barrett ◽  
Raman Malhotra

2011 ◽  
Vol 59 (11) ◽  
pp. 763-766 ◽  
Author(s):  
Zulfu Arikanoglu ◽  
Sami Akbulut ◽  
Murat Basbug ◽  
Fatih Meteroglu ◽  
Ayhan Senol ◽  
...  

1988 ◽  
Vol 36 (4) ◽  
pp. 1496-1499
Author(s):  
Osamu Inoue ◽  
Kunio Ibaraki ◽  
Hiromichi Norimatsu ◽  
Tomoaki Yoshikawa ◽  
Satoshi Tomiyama ◽  
...  

2011 ◽  
Vol 23 (Suppl 2) ◽  
pp. S239 ◽  
Author(s):  
Jimin Chung ◽  
Sun Namkoong ◽  
Ji Hyun Sim ◽  
Joong Sun Lee ◽  
Seung Phil Hong ◽  
...  

The Knee ◽  
2006 ◽  
Vol 13 (1) ◽  
pp. 48-50
Author(s):  
Manickam Rathinam ◽  
David M. Wright ◽  
Juan A. Alonso ◽  
David H. Sochart

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