scholarly journals Primary high grade mucoepidermoid carcinoma of skin and cervical lymphatic affection a rare entity

MOJ Surgery ◽  
2108 ◽  
Vol 6 (4) ◽  
Author(s):  
Zaki Taissoun Aslan ◽  
Martin Granados Garcia ◽  
Kuauhyama Luna Ortiz ◽  
Francisco Javier Guerrero Huerta ◽  
Antonio Gomez Pedraza ◽  
...  
2011 ◽  
Vol 5 ◽  
pp. CPath.S8435 ◽  
Author(s):  
Sepideh Mokhtari ◽  
Saeedeh Mokhtari

Mucoepidermoid carcinoma is the most common malignant tumor of salivary glands. However, it is a rare entity in larynx. Laryngeal cases are frequently misdiagnosed with other malignancies and they are under-reported. So, recognizing the clinical and histological features of this tumor is essential. Laryngeal mucoepidermoid carcinoma can arise in supraglottis, glottis and subglottis. Generally, it presents as a submucosal mass; therefore, progressive symptoms without any identifiable lesion in laryngoscopy must be well considered. The prognosis is somehow dependent on the histological features. In high-grade tumors, recurrence is more common and radical surgery with radiotherapy is recommended. In this paper, we provide a thorough literature review on mucoepidermoid carcinoma in the larynx. The most important distinguishing features of mucoepidermoid carcinoma and its two major differential diagnoses (squamous cell carcinoma and adenosquamous carcinoma) are clearly stated and pitfalls in true diagnosis of this tumor are discussed.


2021 ◽  
pp. 030089162199589
Author(s):  
Zhang Jieli ◽  
Zhou Yunzhi ◽  
Zhang Nan ◽  
Zou Heng ◽  
Wang Hongwu ◽  
...  

Aims: To investigate the efficacy and safety of minimally invasive bronchoscopic interventions for patients with tracheobronchial mucoepidermoid carcinoma (MEC). Methods: Patients with tracheobronchial MEC were included in this retrospective study, and the clinical features, histologic grading, treatments, and cumulative survival rates were calculated. Patients were categorized into child (n = 16) and adult (n = 19) group according to their ages. Histologic grading, treatments, and survival status were compared between the two groups. Results: In pathology, high-grade MEC counts for 6.77% and 42.10% in the child and adult group, respectively. As tumor growth pattern was concerned, 93.33% and 21.05% tumors in the child and adult group present intratracheal type. Multiple bronchoscopic interventions were conducted, including rigid bronchoscopy, argon plasma coagulation (APC), dioxide carbon cryotherapy, and electric loop. Tumors could be removed by multiple bronchoscopic interventions. Bronchoscopy-associated complications were rare, including an oral mucosa injury and a glottis edema. In the child group, one patient underwent left upper lung lobectomy. In the adult group, lobectomy and/or chemotherapy and/or radiotherapy were conducted in seven patients. The 5-year survival rate was 100% and 68.90% in the child and the adult group, respectively. Conclusions: Almost all children have low-grade and intratracheal MEC; 2/5 adults have invasive high-grade MEC. Multiple bronchoscopic interventions are effective in erasing low-grade intratracheal MEC without severe complications. For high-grade invasive MEC, aggressive and comprehensive therapy should be considered.


2012 ◽  
Vol 42 (6) ◽  
pp. 552-555 ◽  
Author(s):  
A. Kanemoto ◽  
Y. Oshiro ◽  
S. Sugahara ◽  
S. Kamagata ◽  
S. Hirobe ◽  
...  

2006 ◽  
Vol 135 (2_suppl) ◽  
pp. P234-P234
Author(s):  
Kevin S Emerick ◽  
Daniel G Deschler ◽  
Richard L Fabian

2014 ◽  
Vol 138 (7) ◽  
pp. 982-985 ◽  
Author(s):  
Whitney A. McCarthy ◽  
Bettye L. Cox

Diagnoses most commonly associated with a unilateral parotid mass include sialadenitis, pleomorphic adenoma, Warthin tumor, and mucoepidermoid carcinoma. However, rare entities, such as intraparotid schwannoma, must be considered in the differential diagnosis. We present a brief literature review that is illustrative of the current difficulty of preoperative diagnosis of intraparotid schwannoma, which is an exceptionally rare entity, with approximately 80 cases described to date. It may mimic common neoplasms and inflammatory salivary gland conditions on fine-needle aspiration and imaging, but is more likely to be associated with the facial nerve. Depending upon the tumor's spatial relationship to the facial nerve and the extent of neurologic dysfunction, the decision may be made to observe the tumor rather than attempt resection. This potential implication for patient management is a critical consideration that highlights the need for timely, appropriate biopsy and diagnosis.


2017 ◽  
Vol 33 (6) ◽  
pp. 678-680 ◽  
Author(s):  
Atul Vats ◽  
Amit Amit ◽  
Paresh Doshi
Keyword(s):  

2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Dario Marcotullio ◽  
Marco de Vincentiis ◽  
Giannicola Iannella ◽  
Bruna Cerbelli ◽  
Giuseppe Magliulo

Introduction. True malignant mixed tumor, also known as carcinosarcoma, is a rare tumor of the salivary gland composed of both malignant epithelial and malignant mesenchymal elements. Frequently carcinosarcoma arises in the background of a preexisting pleomorphic adenoma; however, if no evidence of benign mixed tumor is present, the lesion is known as carcinosarcoma “de novo.” We reported the first case of true malignant mixed tumor of the submandibular gland composed of high grade mucoepidermoid carcinoma associated with osteosarcoma.Case Presentation. A 69-year-old Caucasian male came to our department complaining of the appearance of an asymptomatic left submandibular neoformation progressively increasing in size over 3 months. We opted for surgical treatment. Histological examination confirmed the diagnosis of carcinosarcoma with the coexistence of high grade mucoepidermoid carcinoma and osteosarcoma.Conclusion. To the best of our knowledge, in the true malignant mixed tumor of the submandibular gland, mucoepidermoid carcinoma associated with osteosarcoma has never been previously reported.


2014 ◽  
Vol 43 (8) ◽  
pp. 579-584 ◽  
Author(s):  
Li Siyi ◽  
Liu Shengwen ◽  
Ruan Min ◽  
Yang Wenjun ◽  
Wang Lizheng ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document