scholarly journals Primary thyroid-like low-grade nasopharyngeal papillary adenocarcinoma in a 11-year-old male patient: The first case report in Indonesia

2020 ◽  
Vol 21 ◽  
pp. 200392
Author(s):  
Emilia Theresia ◽  
Ery Kus Dwianingsih ◽  
Hanggoro Tri Rinonce ◽  
Rita Cempaka ◽  
Camelia Herdini ◽  
...  
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Papillary Adenocarcinoma ◽  
Low Grade ◽  
First Case

scholarly journals Low grade nasopharyngeal papillary adenocarcinoma case report from the Middle East

2020 ◽  
Vol 6 (9) ◽  
pp. 1721
Author(s):  
Suzan S. Mohammed ◽  
Hassan H. Ahmad ◽  
Adham A. Ammar ◽  
Waheed Rahman
Keyword(s):  
Case Report ◽  
Middle East ◽  
Treatment Approach ◽  
English Literature ◽  
Papillary Adenocarcinoma ◽  
Low Grade ◽  
Combined Approach ◽  
Rare Type ◽  
First Case ◽  
Left Neck

<p>Nasopharyngeal papillary adenocarcinoma variety is extremely rare type of nasopharyngeal carcinoma. Limited number of cases reported in the literature, with most cases being reported from west and south Asia. We report the first case in English literature from the middle east and south Africa. A young gentleman diagnosed with low-grade nasopharyngeal papillary adenocarcinoma with positive cervical lymph node. He received a combined approach with endoscopic resection of the lesion and concomitant Left neck dissection followed by planned chemoradiotherapy. Through this case report, we would like to share our treatment approach and explore the optimum therapeutic strategies for primary nasopharyngeal papillary adenocarcinomas.</p><p> </p>

scholarly journals Thyroid-like low-grade nasopharyngeal papillary adenocarcinoma: a case report and literature review

2020 ◽  
Vol 9 (7) ◽  
pp. 4457-4463
Author(s):  
Jun Wang ◽  
Zhao-Zhen Chen ◽  
Chen-Lu Lian ◽  
Qin Lin ◽  
San-Gang Wu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Papillary Adenocarcinoma ◽  
Low Grade

scholarly journals Gilbert Syndrome in a Young Ethiopian Man: First Case Report

2021 ◽  
Vol 31 (1) ◽  
Author(s):  
Amir Sultan ◽  
Kibrewossen Kiflu
Keyword(s):  
Case Report ◽  
Liver Function ◽  
Male Patient ◽  
Liver Function Tests ◽  
Prolonged Fasting ◽  
Unconjugated Hyperbilirubinemia ◽  
Gilbert Syndrome ◽  
Function Tests ◽  
First Case

BACKGROUND፡ Gilbert syndrome is a well-recognized condition causing unconjugated hyperbilirubinemia with otherwise normal transaminases and liver function tests. CASE: A 21 year old male patient presented with recurrent episodes of jaundice over four years. The episodes were preceded by stressful conditions and intercurrent illnesses. All laboratory prameters were normal except an unconjugated hyperbilirubinemia. A diagnosis of Gilbert syndrome was made after careful clinical evaluation.CONCLUSION: Recognizing Gilbert syndrome has important clinical implicaitions by avoiding uncessary and expensive workup of patients with jaundice. Mangement entails avoiding stressful conditions and prolonged fasting. 

scholarly journals Spinal Intradural, Extramedullary Ependymoma with Astrocytoma Component: A Case Report and Review of the Literature

2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Gene M. Weinstein ◽  
Knarik Arkun ◽  
James Kryzanski ◽  
Michael Lanfranchi ◽  
Gaurav K. Gupta ◽  
...  
Keyword(s):  
Back Pain ◽  
Case Report ◽  
Lower Back Pain ◽  
Low Grade ◽  
Review Of The Literature ◽  
Pathologic Evaluation ◽  
Lower Back ◽  
Spinal Lesions ◽  
First Case ◽  
Intradural Extramedullary

Ependymomas are common spinal lesions, with the vast majority arising in an intramedullary location. Several cases have been described in the literature of ependymomas in an intradural, extramedullary location. The authors present a case of a 56-year-old female who presented with several weeks of lower back pain and weakness. MRI revealed an intradural, extramedullary enhancing mass at L1-L2. The mass was successfully resected surgically. Pathologic evaluation revealed a low grade glioma with components of both ependymoma and pilocytic astrocytoma with MUTYH G382D mutation. Extramedullary ependymomas are very rare tumors. To the authors’ knowledge, this is the first case of ependymoma/astrocytoma collision tumors described in an extramedullary location.

scholarly journals Gastric mixed adenoneuroendocrine carcinoma case report

2019 ◽  
Vol 7 ◽  
pp. 2050313X1982891
Author(s):  
Miguel Angel Moyón Constante ◽  
Fernando Xavier Moyón Constante ◽  
Jorge Fernando Tufiño ◽  
Andres Cárdenas Patiño ◽  
Gabriel Alejandro Molina ◽  
...  
Keyword(s):  
Case Report ◽  
World Health ◽  
Low Grade ◽  
Radical Gastrectomy ◽  
Upper Endoscopy ◽  
Mixed Adenoneuroendocrine Carcinoma ◽  
First Case ◽  
The World ◽  
Medical Teams ◽  
Health Organization

Mixed adenoneuroendocrine carcinomas are rare tumors that contain both an exocrine and an endocrine component. Since the latest classification by the World Health Organization and with the aid of immunostaining, more mixed adenoneuroendocrine carcinomas are now identified and diagnosed. Nonetheless, our knowledge of these tumors is still limited, notably concerning gastric variants, as the cases reported in the literature are very limited. The clinical and surgical treatment, including the chemotherapy schemes, the prognosis, and recurrence still represent challenges for the medical teams. We present the case of a 62-year-old woman. After an upper endoscopy revealed multiple polyps and a low-grade neuroendocrine tumor, a D2 radical gastrectomy was performed. A low output esophageal anastomotic leak was discovered in the postoperative period and successfully managed. Pathology revealed a gastric mixed adenoneuroendocrine carcinoma, the first case of this kind reported in Ecuador. Patient is doing well and under constant surveillance up until her 13th postoperative month.

scholarly journals LOW-GRADE MYOFIBROBLASTIC SARCOMA OF THE LARYNX: CASE REPORT AND REVIEW OF LITERATURE

2014 ◽  
Vol 57 (4) ◽  
pp. 162-164 ◽  
Author(s):  
Petr Kordač ◽  
Dimitar Hadži Nikolov ◽  
Katarína Smatanová ◽  
David Kalfeřt
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Male Patient ◽  
Neck Region ◽  
Clinicopathological Characteristics ◽  
Low Grade ◽  
Review Of Literature ◽  
Head And Neck Region ◽  
Myofibroblastic Sarcoma ◽  
Male Predominance

Low-grade myofibroblastic sarcoma (LGMS) is a very rare, atypical myofibroblastic tumor with fibromatosis-like features with predilection mostly in head and neck region. LGMS occurs primarily in adult patients with a slight male predominance. Only few cases of LGMS affecting the larynx have been reported in literature to this date. We describe a case of low-grade myofibroblastic sarcoma of the larynx in a 40-year-old male patient. The clinicopathological characteristics, immunohistochemical findings and treatment are discussed.

scholarly journals Complete endoscopic resection of low-grade nasopharyngeal papillary adenocarcinoma: a case report

2020 ◽  
Author(s):  
Inaê M. Compagnoni ◽  
Lorena A. Lamounier ◽  
Letícia Fontanini ◽  
Gabriela T. Silveira ◽  
Francesca M. Faria ◽  
...  
Keyword(s):  
Case Report ◽  
Endoscopic Resection ◽  
Papillary Adenocarcinoma ◽  
Low Grade
Sign in / Sign up

Export Citation Format

Share Document