2.Low-grade myofibroblastic sarcoma of the palate.
Tomohiro YAMADA ; Tomohide YOSHIMURA ; Naoya KITAMURA ; Eri SASABE ; Seiji OHNO ; Tetsuya YAMAMOTO
International Journal of Oral Science 2012;4(3):170-173
Low-grade myofibroblastic sarcoma (LGMS) is a rare, malignant tumor with myofibroblastic differentiation. Despite it being classified as a distinct entity by the World Health Organization, a few cases were reported in the oral and maxillofacial region. Here, a LGMS developed on the palate of a 73-year-old man who presented with a 1-cm tumor on the posterior border of the palate. Based on the histological and immunohistochemical features, a diagnosis of LGMS was established. The tumor was resected, and no recurrence was observed over 2 years. Although the tongue is the most preferred site for LGMS, it may occur in any region of the oral cavity.
Aged
;
Humans
;
Male
;
Myofibroblasts
;
pathology
;
Osteosarcoma
;
pathology
;
surgery
;
Palatal Neoplasms
;
pathology
;
surgery
;
Palate, Hard
;
pathology
3.Malignant Myoepithelioma of the Palate: A Case Report with Review of the Clinicopathological Characteristics.
Mustafa Fuat ACIKALIN ; Ozgul PASAOGLU ; Hamdi CAKLI ; Kezban GURBUZ ; Funda CANAZ
Yonsei Medical Journal 2009;50(6):848-851
A malignant myoepithelioma is one of the rarest salivary gland neoplasms which may either arise de novo or develop within a preexisting pleomorphic adenoma or benign myoepithelioma. The parotid gland is the most common primary site and the palate the most common intra-oral site of occurrence. Herein is present a case of a malignant myoepithelioma arising in the hard palate of a 79-year-old woman. The lesion had been examined by biopsy at another hospital, and diagnosed as a poorly differentiated squamous cell carcinoma. The patient underwent a wide local tumor resection. Examination of the resection specimen showed the characteristic histopathological and immunohistochemical features of a malignant myoepithelioma. Five months after the operation, the patient was well without evidence of recurrence or metastasis.
Aged
;
Female
;
Humans
;
Immunohistochemistry
;
Myoepithelioma/*diagnosis/*pathology/surgery
;
Palatal Neoplasms/*diagnosis/*pathology/surgery
;
Palate/*pathology/*surgery
4.Some important aspects of the palatal pleomorphic adenoma.
Singapore medical journal 1981;22(6):358-360
5.Large mixed tumors of salivary: two cases reports.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;28(21):1714-1715
It is rare that large mixed tumors of salivary gland located in the nose and uvula. The patient who had mixed tumors of salivary gland at nose found exophytic growth tumor for half a year. The other patient who had mixed tumors of salivary gland at uvula felt swallowing foreign body sensation for one year, and dysphagia for one month. After surgical resection, the symptoms disappear.
Adenoma, Pleomorphic
;
complications
;
pathology
;
Deglutition
;
Deglutition Disorders
;
etiology
;
Humans
;
Nose Neoplasms
;
pathology
;
Palatal Neoplasms
;
pathology
;
Salivary Gland Neoplasms
;
complications
;
pathology
;
Uvula
;
pathology
6.Analysis on the relationship between tensor veli palatini and secretory otitis media in patients with nasopharyngeal carcinoma after radiotherapy.
Yiling GAO ; Anzhou TANG ; Jin LIU ; Xiaoming WANG ; Guangyao HE ; Zhigang MIN
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2010;24(16):743-745
OBJECTIVE:
The analyze the relationship between secretory otitis media (SOM) and injury of tensor veli palatini (TVP) muscle injury after radiotherapy, then to explore the pathogenesis of SOM in patients with nasopharyngeal carcinoma (NPC) after radiotherapy.
METHOD:
The cross section area (CSA) of TVP and medial pterygoid (MP) muscle were measured in MRI of 32 patients with NPC before and after radiotherapy, meanwhile the incidence of SOM were surveyed after radiotherapy, then to analyze the relationship between the change of TVP and the incidence of SOM after radiotherapy.
RESULT:
Of 48 ears without SOM before radiotherapy, 27 ears developed post-irradiation SOM, including 24 ears with TVP atrophy and 3 ears without TVP atrophy, and 21 ears had no post-irradiation SOM, including 8 ears with TVP atrophy and 13 ears without TVP atrophy. chi2 test showed significant difference (P < 0.01). It indicated that post-irradiation SOM have correlation with TVP atrophy. The more possibility of TVP atrophy occurred after long time radiotherapy.
CONCLUSION
The atrophy of TVP in patients with NPC usually occurs 6 months after radiotherapy, and this may result in the post-irradiation SOM. The pathogenesis of post-irradiation SOM need further study functionally.
Adult
;
Aged
;
Female
;
Humans
;
Male
;
Middle Aged
;
Nasopharyngeal Neoplasms
;
radiotherapy
;
Otitis Media with Effusion
;
etiology
;
Palatal Muscles
;
pathology
;
Palate, Soft
;
pathology
7.Squamous papilloma: case report and review of literature.
Prashant P JAJU ; Prashant V SUVARNA ; Rajiv S DESAI
International Journal of Oral Science 2010;2(4):222-225
Squamous papillomas are common lesions of the oral mucosa with a predilection for the mucosa of the hard and soft palate. As an oral lesion, it raises concern because of its clinical appearance, which may mimic exophytic carcinoma, verrucous carcinoma or condyloma acuminatum. Its pathogenesis is related to human papilloma virus but there is controversy regarding its viral origin. We present a case of squamous papilloma presenting as oral lesion along with a review of the literature.
Adult
;
Condylomata Acuminata
;
diagnosis
;
Diagnosis, Differential
;
Female
;
Humans
;
Hyperplasia
;
diagnosis
;
Mouth Mucosa
;
pathology
;
Palatal Neoplasms
;
pathology
;
Palate, Hard
;
pathology
;
Papilloma
;
pathology
;
Papillomavirus Infections
;
pathology
;
Xanthomatosis
;
diagnosis
8.Metastatic tumors in the sellar and parasellar regions: clinical review of four cases.
Hyeong Joong YI ; Choong Hyun KIM ; Koang Hum BAK ; Jae Min KIM ; Yong KO ; Suck Jun OH
Journal of Korean Medical Science 2000;15(3):363-367
Metastatic tumors in the sellar and parasellar regions are uncommon and rarely detected in clinical practice. We present four cases of sellar and parasellar metastatic tumors, which metastasized from distant organ in one case and extended directly from adjacent structures in three. Common presenting symptoms were cranial neuropathies, headache and facial pain. Invasion into the cavernous sinus was noted in all cases. We report rare cases of sellar and parasellar metastases. Also, we should consider the possibility of metastasis in these regions for patients who showed the above clinical presentations in systemic cancer patients. In extensive diseases, transient symptomatic relief could be obtained by direct surgical management, even in restricted degree.
Adenocarcinoma/therapy
;
Adenocarcinoma/radiography
;
Adenocarcinoma/pathology*
;
Adult
;
Breast Neoplasms/radiography
;
Breast Neoplasms/pathology*
;
Carcinoma, Infiltrating Duct/therapy
;
Carcinoma, Infiltrating Duct/radiography
;
Carcinoma, Infiltrating Duct/pathology*
;
Case Report
;
Female
;
Human
;
Magnetic Resonance Imaging/methods
;
Male
;
Middle Age
;
Nasopharyngeal Neoplasms/therapy
;
Nasopharyngeal Neoplasms/radiography
;
Nasopharyngeal Neoplasms/pathology*
;
Palatal Neoplasms/therapy
;
Palatal Neoplasms/radiography
;
Palatal Neoplasms/pathology*
;
Sella Turcica*
;
Skull Neoplasms/therapy
;
Skull Neoplasms/secondary*
;
Skull Neoplasms/physiopathology
9.Ectomesenchymal chondromyxoid tumor: a comprehensive updated review of the literature and case report.
Astrid TRUSCHNEGG ; Stephan ACHAM ; Lumnije KQIKU ; Norbert JAKSE ; Alfred BEHAM
International Journal of Oral Science 2018;10(1):4-4
Prompted by a unique case of an ectomesenchymal chondromyxoid tumor (ECT) of the palate in a 54-year-old female, we reviewed the English and German literature on this entity until the end of 2016 using PubMed. The search produced 74 lingual cases with a nearly equal sex distribution and a mean age of 39.3 years, and two extra-lingual cases sharing histological and immunohistological features including nodular growth, round, fusiform or spindle-shaped cellular architecture, and chondromyxoid stroma. Immunophenotyping showed the majority of cases to be positive for glial fibrillary acidic protein (GFAP), S-100 protein, glycoprotein CD57, pancytokeratin (AE1/AE3), and smooth muscle actin (SMA); in isolated cases there was molecular-genetic rearrangement or gain of Ewing sarcoma breakpoint region 1 (EWSR1) but no rearrangement of pleomorphic adenoma gene 1 (PLAG1). At present, ectomesenchymal cells that migrate from the neural crest are considered to play a pivotal role in tumor origin. All cases had a benign course, although there were three recurrences. Because of the rarity of this tumor and the need for differential diagnostic differentiation from myoepithelioma and pleomorphic adenoma, both oral surgeons and pathologists should be aware of this entity.
Biomarkers, Tumor
;
analysis
;
Chondroma
;
pathology
;
surgery
;
Diagnosis, Differential
;
Female
;
Humans
;
Immunophenotyping
;
Mesenchymoma
;
pathology
;
surgery
;
Middle Aged
;
Myoepithelioma
;
pathology
;
surgery
;
Palatal Neoplasms
;
pathology
;
surgery
10.A Case of NK/T-Cell Lymphoma Complicated by a Squamous Cell Carcinoma of Hard Palate during Combination Chemotherapy and Radiation Therapy.
Hang Lak LEE ; Myung Ju AHN ; Jung Hye CHOI ; Woon Hyun JUN ; Young Yuel LEE ; In Soon KIM ; Il Young CHOI ; Se Jin JANG ; Yong Wook PARK
The Korean Journal of Internal Medicine 2002;17(1):69-72
NK/T-cell lymphoma, which often shows an angiocentric growth pattern, is a distinct clinicopathologic entity highly associated with Epstein-Barr virus. The disease is characterized by a destruction of the upper respiratory tract, particularly the nasal cavity, palate and paranasal sinuses. Interestingly, NK/T-cell lymphoma is closely linked to a variety of complications, such as hemophagocytic syndrome, second primary cancer, sepsis and bleeding. Here we report a case of a 50-year-old man diagnosed initially as NK/T-cell lymphoma of the oropharynx and who developed a second primary carcinoma of the hard palate during combination chemotherapy and radiation therapy.
Carcinoma, Squamous Cell/*pathology/therapy
;
Case Report
;
Combined Modality Therapy
;
Fatal Outcome
;
Human
;
Killer Cells, Natural
;
Lymphoma, T-Cell/*pathology/therapy
;
Male
;
Middle Age
;
Neoplasms, Second Primary/*pathology/therapy
;
Oropharyngeal Neoplasms/*pathology/therapy
;
Palatal Neoplasms/*pathology/therapy