Although there has been considerable advancement in treatment techniques but still there are some illnesses that continue to exhibit a rather poor curability, such as thymoma. This report highlights the benefit of octreotide and prednisolone therapy in a 15-year-old girl, who was diagnosed with inoperable thymus carcinoma, with chemotherapy and radiotherapy being the last resort. The detection of type 2 somatostatin receptors on the surface of the tumor justified the introduction of treatment with somatostatin analog and prednisolone. Fortunately, after 6 months of this treatment, the tumor showed partial regression. However, 2 months later, somatostatin receptor negative metastases appeared; therefore, a switch over to imatinib became essential, because the tumor was CD-117 positive. Despite the therapy change, the patient's condition deteriorated owing to tumor progression.
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http://dx.doi.org/10.1097/MPH.0b013e318159a535 | DOI Listing |
World J Clin Cases
September 2022
Clinical Trial Center, National Medical Products Administration Key Laboratory for Clinical Research and Evaluation of Innovative Drugs, Department of Thoracic Oncology, West China Hospital, Sichuan University, Cheng Du 610041, Sichuan Province, China.
Background: Salivary gland cancer is a rare disease in which cancer cells form in the tissues of the salivary glands. It mostly occurs in the glands that have secretion functions, such as the parotid gland, sublingual gland and submandibular gland. This is very rare when it occurs in other nonsecreting glands.
View Article and Find Full Text PDFStrahlenther Onkol
September 2021
Department of Oncology and Radiotherapy, Charles University in Prague, Faculty of Medicine and University Hospital in Pilsen, alej Svobody 80, 304 60, Pilsen, Czech Republic.
Carcinoma showing thymus-like elements (CASTLE) is an extremely rare malignant tumor of the thyroid gland and soft tissues of the neck with favorable prognosis. Histological features of the CASTLE are similar to thymic carcinoma, and it is assumed that it arises from the ectopic thymic tissue or the remnants of branchial pouches. The optimal treatment strategy is still uncertain because of the rarity of the tumor.
View Article and Find Full Text PDFCancer Radiother
April 2021
Department of radiation oncology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China. Electronic address:
Purpose: To evaluate the safety and efficacy of Cyberknife® (CK) for the treatment of primary or recurring thymic tumours.
Materials And Methods: We retrospectively reviewed 12 patients (16 tumour lesions) with primary or recurring thymic tumours who were treated with CK between March 2008 and October 2017. Their data was stored in prospectively collected database.
Medicine (Baltimore)
January 2020
Institute for Applied Epistemology and Medical Methodology at the University of Witten/Herdecke.
Rationale: Thymic neuroendocrine tumor (TNET) is very rare and characterized by a tendency to invade adjacent structures, frequent metastasis, resistance to therapy, and a poor prognosis. Viscum album extracts (VAE) have shown immunological, apoptogenic, and cytotoxic properties.
Patient Concerns: A 54-year-old Peruvian man was suffering from constant fatigue, cough, dyspnea, and fever for a couple of months.
North Clin Istanb
August 2018
Emergency and First Aid Program, Vocational School of Health Services KTO Karatay University, Konya, Turkey.
Cushing's syndromes (CS) due to thymic carcinoids are rarely seen. In this text, a case with CS due to ectopic adrenocorticotropic hormone (ACTH) secreting atypical thymic carcinoid tumor is presented. A 50-year-old Turkish male patient was admitted to our emergency department with typical CS features.
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