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Regret for the inconvenience: we are taking measures to prevent fraudulent form submissions by extractors and page crawlers. Received: May 09, Published: April 11, Citation: Khairwa A. Sarcomatoid carcinoma of the tongue: a rare malignancy in an unusual site —a case report with uncommon history.

Multifocal spindle cell hemangioma: Report of two cases

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Spindle cell carcinoma of the head and neck region: treatment and outcomes of 15 patients

Spindle cell hemangioma, formerly known as spindle cell hemangioendothelioma was first described in and was initially considered to be a low-grade angiosarcoma. In , its benign behavior was recognised and the name spindle cell hemangioma was proposed. The tumor originates from blood vessels and recently, lymphatic origin has been suggested. We present two cases of multifocal spindle cell hemangiomas. One case was successfully treated with sclerotherapy suggesting that this can be an alternative treatment which is less invasive and has better long-term results. The first case was a year-old girl with a 4-year history of multiple violaceous and reddish cutaneous and subcutaneous nodules on the right ankle and foot [Figure - 1].

According to previous studies, spindle cell carcinoma SpCC is an unusual form of divergent differentiated squamous cell carcinoma SCC , which consists of elongated spindle epithelial cells and resembles a sarcoma 1. SCC, with the spindle cell component, is an uncommon phenomenon and a rare type of malignant tumor. It is also termed as a sarcomatoid carcinoma, pseudosarcoma, pleomorphic carcinoma and sarcomatous carcinoma 2 , 3. There are numerous reports describing the clinical and pathological findings of SpCC in the head and neck 4 — 7 , with the majority described as being located in the oral cavity, larynx, tonsils and pharynx. However, SpCC occurs elsewhere in the body, such as the skin, lungs and breasts, and the symptoms vary according to the site. The histogenesis of SpCC has been the subject of debate for many decades.


Spindle cell carcinoma (SpCC) is a rare and unusual biphasic malignant findings of SpCC in the head and neck; however, this type of tumor.


Otolaryngology-ENT Research

Background: Sarcomatoid carcinoma is a biphasic tumour comprising both of malignant epithelial and mesenchymal elements derived monoclonally from same stem cells. Only few studies have been published and needs more understanding to establish treatment guidelines. The aim of this study was to review the cases of carcinosarcoma arising from mucosal sites of head and neck and study their clinical, histological and Immunohistochemical features.

Providing cutting-edge scholarly communications to worldwide, enabling them to utilize available resources effectively. We aim to bring about a change in modern scholarly communications through the effective use of editorial and publishing polices. Health Science University, Dr.

Giant-cell tumors of soft tissue in the head and neck: A review article

Undifferentiated head and neck tumors: the contribution of immunohistochemical technique to differential diagnosis. They can arise in mucosa as well as in salivary glands, soft tissues or lymph nodes. Suitable therapy and prognosis for each case depends upon precise histopathological diagnosis. The occurrence of these tumors in our service and the way in which they were distributed according to cell pattern, patient's age and tumor location was also evaluated. The final diagnosis was achieved after new analysis in conjunction with biopsies stained using the hematoxylin-eosin technique. They were most prevalent during the seventh decade of life

This review article aims to recognize the characteristics of this rare tumor along with a favorable way to diagnose and treat. This tumor involves both sexes at any age. Histopathology in many cases revealed the presence of mononuclear cells and spindle cells. Immunohistochemistry was positive in many cases for CD Complete excision was the most accepted management technique; however, few cases reported recurrence and metastasis. Post-operative radiology is suggested to prevent local recurrence and in case of incomplete excision of the tumor.

Metrics details. Spindle cell rhabdomyosarcoma of the head and neck is a very rare tumor in adults. We report on one case with long-term survival. A year-old nonsmoking Caucasian man presented in June with a painless swelling under his tongue. A diagnosis of a soft tissue sarcoma, and a myofibrosarcoma in particular, was made via biopsy.


WHO Blue Books in PDF: Pathology and Genetics of Head and Neck Tumours. Editors. Coordinating Editor. Layout Spindle cell carcinoma is characterized.


2 Comments

Derachecheng 12.03.2021 at 04:31

PDF | Sarcomatoid carcinomas are biphasic tumors proven to be monoclonal dedifferentiated forms of conventional squamous carcinomas.

JГјrgen C. 20.03.2021 at 02:26

PDF | Giant-cell tumor of soft tissue (GCT-ST) is a rare neoplasm that was first We reviewed 12 cases of GCT-ST in the head and neck. Histopathology in many cases revealed the presence of mononuclear cells and spindle cells. editor. 22/M Intermittent. headache. over the left. temporal area.

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