Pharyngeal cyst arising from second branchial cleft

1989 ◽  
Vol 103 (10) ◽  
pp. 964-965 ◽  
Author(s):  
T. Takimoto ◽  
Y. Akemoto ◽  
R. Umeda
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Intraoral Approach ◽  
Branchial Cleft ◽  
The Right

AbstractA rare case of pharyngeal cyst arising from the second branchial cleft in a 14-year-old boy is described. A cyst located in the right posterolateral wall of the oropharynx was completely removed by an intraoral approach. Histopathological examination revealed that the cyst was lined with columnar (respiratory type) epithelium.

scholarly journals Desmoplastic Fibroma and Cemento Ossifying Fibroma of The Anterior Maxilla: A Rare Case Report

2021 ◽  
Vol 24 (1) ◽  
pp. 21-27
Author(s):  
Victor Pakpahan ◽  
Eky Nasuri ◽  
Vera Julia
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Neck Region ◽  
The Body ◽  
Ossifying Fibroma ◽  
Desmoplastic Fibroma ◽  
Anterior Maxilla ◽  
Main Complaint ◽  
Rare Case Report ◽  
The Right

Tumors located in the maxillofacial part of the body were classified by WHO in 2017 and among these are intraosseous form of fibromatosis known as Desmoplastic and Cemento-ossifying fibromas. These tumors usually occur in the head and neck region, especially in the mandible and are relatively rare in the maxilla. Meanwhile, this study aims to discribe a rare case of the cemento ossifying fibroma that had been previously diagnosed as desmoplastic fibroma with a mass tumor in the anterior of the maxilla. A 22 years old female reported to the Cipto Mangkusumo Hospital with the main complaint of a lump in the right side of the upper jaw which appeared 2 years prior to the operation. In April 2017, the patient had a biopsy in Tarakan Hospital and the result was a desmoplastic fibroma. Due to the lump enlargement, the patient was admitted to RSCM in July 2019 and had biopsy incision with a diagnosis of cemento ossifying fibroma which was confirmed by the histopathological examination and histology report. The resection of the right part of maxilla was conducted alongside with reconstruction using the free fibular flap. Moreover, cemento ossifying fibroma and desmoplastic fibroma shared similar features, namely, clinical, histological and radiological features which are important in establishing the diagnosis and treatment of patient. Hence, extensive enucleation or resection is required due to the progressive nature of the tumor to prevent the potential for further recurrences.

A RARE CASE REPORT OF PRIMARY NEUROENDOCRINE CARCINOMA OF BREAST

2021 ◽  
pp. 15-16
Author(s):  
Rahmath Unissa ◽  
Amreen Unissa ◽  
M. Bhavani
Keyword(s):  
Case Report ◽  
Clinical Examination ◽  
Rare Case ◽  
Histopathological Examination ◽  
Radical Mastectomy ◽  
Lower Quadrant ◽  
Axillary Clearance ◽  
Rare Case Report ◽  
Trucut Biopsy ◽  
The Right

we report a case of 51 year old lady, presented with complaints of hard lump in the right breast.On clinical examination lump of size 4x3cms in outer lower quadrant was noted. Ultrasonographic imaging showed evidence of 3x2cms ill dened hypoechoic lesion with spiculated margins and microcalcications. Trucut biopsy was done and histopathological report was given as Suspicious for malignancy which was followed by modied radical mastectomy with axillary clearance. Histopathological examination and Immunohistochemistry(IHC) was done.

scholarly journals Lymphoepithelial Cyst of the Hypopharynx

1995 ◽  
Vol 2 (1) ◽  
pp. 53-56 ◽  
Author(s):  
Masahiro Kawaida ◽  
Hiroyuki Fukuda ◽  
Akihiro Shiotani ◽  
Naoyuki Kohno
Keyword(s):  
Mucous Membrane ◽  
Surgical Procedure ◽  
Rare Case ◽  
Histopathological Examination ◽  
Lymphoepithelial Cyst ◽  
Medial Region ◽  
Piriform Sinus ◽  
Direct Laryngoscope ◽  
The Right

A rare case of lymphoepithelial cyst formed in the piriform sinus of the hypopharynx is reported. Histopathological examination revealed a lymphoepithelial cyst. It was removed by laryngomicrosurgical technique using a side-opened direct laryngoscope. Because this cyst was wide-based on the antero-medial region in the right piriform sinus of the hypopharynx, the mucous membrane around the cyst was incised electrosurgically and then detached to facilitate removal. In this paper, we describe our surgical procedure for removing the cyst in this case and discuss the possible causes of the disease.

Neurofibroma of Soft Palate: A Rare Case Report

2013 ◽  
Vol 5 (2) ◽  
pp. 19-20
Author(s):  
SG Smitha ◽  
Smitha Soubhagya Gangaraj ◽  
Lakshmi Shantharam ◽  
Suguna Vijay
Keyword(s):  
Case Report ◽  
Soft Palate ◽  
Rare Case ◽  
Histopathological Examination ◽  
English Literature ◽  
Rare Tumor ◽  
Fourth Case ◽  
Intraoral Approach ◽  
Rare Case Report

ABSTRACT Neurofibroma of soft palate is a rare tumor with this report being the fourth case reported in English literature. We are reporting this case of isolated neurofibroma of soft palate for its rarity. The mass was excised by intraoral approach without prior tracheostomy. Histopathological examination showed features of neurofibroma with secondary changes.

scholarly journals Lymphoepithelial Cyst in the Palatine Tonsil

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Fatih Bingöl ◽  
Hilal Balta ◽  
Buket Özel Bingöl ◽  
Recai Muhammet Mazlumoğlu ◽  
Korhan Kılıç
Keyword(s):  
Magnetic Resonance Imaging ◽  
Rare Case ◽  
Histopathological Examination ◽  
Cystic Mass ◽  
Palatine Tonsil ◽  
Lateral Part ◽  
Lymphoepithelial Cyst ◽  
Resonance Imaging ◽  
Tonsil Surgery ◽  
The Right

Lymphoepithelial cyst (LEC) is the most commonly encountered congenital neck pathology in the lateral part of the neck. A 66-year-old woman presented to the ENT clinic due to difficulty in swallowing persisting for approximately 1 year. Magnetic resonance imaging revealed a cystic mass at right tonsil. Surgery was performed due to this unilateral tonsillar mass, which was excised together with the right tonsil. LEC was diagnosed at histopathological examination. LEC in the palatine tonsil is rare, and only a few cases have been reported in the literature. We report a rare case of LEC in the palatine tonsil.

scholarly journals Perforated High-Grade Mixed Neuroendocrine Nonneuroendocrine Neoplasm of Cecum: Unusual Presentation of Rare Disease

2021 ◽  
pp. 1-6
Author(s):  
Gunasekaran Gopalakrishnan ◽  
Bheemanathi Hanuman Srinivas ◽  
Biju Pottakkat ◽  
Senthil Gnanasekaran ◽  
Raja Kalayarasan
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Psoas Muscle ◽  
Right Hemicolectomy ◽  
Resected Specimen ◽  
Radiological Findings ◽  
En Bloc ◽  
En Bloc Excision ◽  
Bloc Excision ◽  
The Right

Mixed neuroendocrine nonneuroendocrine neoplasms (MiNENs) are rare neoplasms of the gastrointestinal tract, where the neuroendocrine as well as the nonneuroendocrine components each comprise at least 30% of the tumor. Of all cases of colorectal malignancies, MiNENs constitute around 3–9.6%, with only a few cases reported to be arising in the cecum. Since majority present with nonspecific clinical and radiological findings, its diagnosis preoperatively is almost impossible and these are usually diagnosed after histopathological examination of the resected specimen. Owing to the rarity of these tumors as well as lack of complete molecular characterization, optimal treatment remains unestablished. We, here, report a rare case of MiNENs of the cecum infiltrating the right psoas muscle and presenting with perforation for which right hemicolectomy and en bloc excision of the involved psoas muscle was done followed by adjuvant chemotherapy.

scholarly journals Malignant transformation of pleomorphic xanthoastrocytoma: case report

2003 ◽  
Vol 61 (1) ◽  
pp. 104-106 ◽  
Author(s):  
Oswaldo Ignácio de Tella Jr ◽  
Marco Antonio Herculano ◽  
Mirto Nelso Prandini ◽  
João Norberto Stavale ◽  
Paulo Henrique Aguiar
Keyword(s):  
Case Report ◽  
Malignant Transformation ◽  
Temporal Lobe ◽  
Rare Case ◽  
Histopathological Examination ◽  
Pleomorphic Xanthoastrocytoma ◽  
The Right

We report a case of a pleomorphic xantoastrocytoma which manifested itself as a cystic isodense lesion in the right fronto-temporal lobe in a 26 year-old woman. It appeared as a soft yellow tumor with cystic cavities on surgery. Five months after this surgery, the patient was submitted to a new operation, which revealed a friable tumor, easily differentiated from the normal parenchyma, with cystic components. The histopathological examination demonstrated pleomorphic xanthoastrocytoma with malignant transformation. Histologically, the tumor at first procedure was composed of pleomorphic astrocytes with multinucleated and foamy cells. A rare case of malignant transformation in pleomorphic xanthoastrocytoma is presented, discussed and illustrated in this paper.

scholarly journals Emphysematous Pyelonephritis in Patient with Diabetes and Renal Cell Carcinoma

2015 ◽  
Vol 1 (1) ◽  
pp. 52-57
Author(s):  
Bambang Soeprijanto ◽  
Wajoe Djatisoesanto ◽  
Etty Hary Kusumastuti
Keyword(s):  
Renal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Solid Tumor ◽  
Renal Cell ◽  
Rare Case ◽  
Histopathological Examination ◽  
Renal Ultrasound ◽  
Emphysematous Pyelonephritis ◽  
The Right ◽  
Upper Abdomen

Emphysematous pyelonephritis (EPN) usually happens in diabetes. It is reported a correlation between the Renal Cell Carcinoma (RCC) with diabetes. This is a rare case of PEN and RCC in diabetes which occur simultaneously. We present a case of 51 year old male referred with right ?ank mass and medical history of diabetic disease. Renal ultrasound revealed a solid tumor at the upper pole of the right kidney. Plain abdominal X-ray showed a lot of gas, fecal material, and patches of  alcifcation in the right upper abdomen. On abdominal computed tomography found a collection of gas located in the upper right abdomen. An irregular solid tumor detected at the upper pole of the right kidney. The tumors was obtained at surgery and  emphysematous pyelonephritis was found and then nephrectomy performed. Histopathological examination revealed a Renal Cell Carcinoma besides emphysematous pyelonephritis. The patient had no postoperative serious complications during his hospital stay and his symptoms resolved completely. We report the rare case with an occurrence of EPN and RCC simultaneously in diabetes.

scholarly journals A Rare Case of Angiofibroma Mimicking Fibrous Epulis in Posterior Gingival Mucosa

2021 ◽  
Vol 55 (8) ◽  
Author(s):  
Annete Nabila ◽  
Ni Putu Mira Sumarta ◽  
Okky Prasetio
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Excisional Biopsy ◽  
Definitive Diagnosis ◽  
Benign Tumors ◽  
Histopathological Analysis ◽  
Clinical Appearance ◽  
Gingival Mucosa ◽  
The Right ◽  
Superficial Soft Tissue

Angiofibromas are highly vascular, locally aggressive but histologically benign tumors. A 40-year-old woman complaint of pedunculated mass in the right gingiva of the posterior region since 7 months earlier. Surgical excisional biopsy under general anesthesia was performed. Histopathological examination showed an angiofibroma. Angiofibromas are localized in the superficial soft tissue and the gingiva could have a similar clinical appearance as an epulis. Definitive diagnosis was determined through histopathological analysis.

scholarly journals Intra-testicular epidermoid cyst: a rare case report with clinico-radiological dilemma

2017 ◽  
Vol 4 (4) ◽  
pp. 1487
Author(s):  
Gireesha Rawal ◽  
Preeti Sharma ◽  
Surbhi Goyal ◽  
Amit Kumar Yadav ◽  
Ashish Kumar Mandal
Keyword(s):  
Epidermoid Cyst ◽  
Rare Case ◽  
Histopathological Examination ◽  
Benign Lesion ◽  
Testicular Neoplasm ◽  
Mri Findings ◽  
Elderly Male ◽  
Normal Limits ◽  
Rare Case Report ◽  
The Right

Intra-testicular epidermoid cyst of testis is a benign tumour and accounts for 1-2% of all testicular neoplasms. It is a benign lesion, and should be distinguished from dermoid cyst or teratoma, which have a considerable malignant potential. We describe a rare case of testicular epidermoid cyst in an elderly male presenting with gradually increasing testicular mass since 8 months. Local examination revealed a non-tender, irregular, hard mass in the right testis. All routine laboratory investigations along with tumour markers were within normal limits. Ultrasound showed features of a testicular neoplasm following which orchidectomy was performed. Grossly, cut surface of testis showed a cyst measuring 4x2x1cm and microscopic examination revealed features of an epidermoid cyst. Extesive sampling excluded the possibility of a teratomatous focus. This case is described owing to the rarity of this neoplasm and the unusual clinico-radiological presentation. The pre-operative diagnosis of this tumour can be made if characteristic sonographic and MRI findings are obtained in the absence of which these masquerade neoplastic lesions. Histopathological examination thus is vital for a decisive diagnosis.

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