Teratomas are germ cell tumors, manifested with a great variety of clinical features; the most common extragonadal site is the anterior mediastinum. In this case, we report the patient with a large mature mediastinal teratoma with several components of ectodermal and endothermal epithelium. A 24-year-old female patient presented with history of persistent chest pain and progressively aggravating dyspnea for the previous 3 months. A chest X-ray showed a large opacity of the entire left hemithorax. Transcutaneous needle aspiration revealed a purulent fluid. The tube thoracostomy was introduced and the effusion was evacuated. Some weeks later, patient was seen in emergency for persistent cough and lateral chest pain. CT scan revealed a mass of the left hemithorax. The mass showed heterogeneous density, without compressing mediastinum great vessels and left hilar structures. Lipase value was elevated in needle aspiration. The patient underwent a total resection of the mediastinum mass via a left posterolateral thoracotomy. Microscopy revealed a mature teratoma with cystic structures. The patient subsequently made a full recovery. This case provide benign mediastinal teratoma with total atelectasis of left lung and elevated lipase value in needle transcutaneous aspiration; this event is explained by pancreatic component in the cystic tumor. Total removal of the tumor is adequate treatment for this type of teratoma and the prognosis is excellent.
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http://dx.doi.org/10.1155/2016/7869476 | DOI Listing |
Front Oncol
February 2025
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, United States.
Introduction: We report for the first time a case of a postpubertal patient presenting with a metastatic prepubertal-type testicular teratoma.
Case Discussion: A 29-year-old male with a history of corrected unilateral cryptorchidism presented with progressive bilateral lower extremity edema. Imaging revealed an inferior vena cava thrombus associated with a complex mass.
Am J Surg Pathol
March 2025
Department of Pathology and Laboratory Sciences, UC Davis Medical Center, Sacramento, CA.
Somatic malignancy arising in ovarian mature cystic teratoma (MCT) is a relatively rare phenomenon with an estimated incidence ranging from 0.17% to 5.5%.
View Article and Find Full Text PDFZhonghua Wai Ke Za Zhi
March 2025
Department of General Surgery, the Children's Hospital Affliated to Xiangya School of Medicine(Hunan Children's Hospital), Central South University, Changsha 410000, China.
To summarize the clinical traits, diagnostic and therapeutic experiences of pancreatic tumors in children. This is a retrospective case series study. According to inclusion and exclusion criteria, clinical data of 35 children with primary pancreatic tumors who were treated at the Department of General Surgery, the Children's Hospital Affiliated to Xiangya School of Medicine, Central South University were collected from January 2010 to June 2023.
View Article and Find Full Text PDFUrol Case Rep
March 2025
Department of Pediatric Surgery, Fattouma Bourguiba Hospital, Monastir, Tunisia.
Most multicystic dysplastic kidneys (MCDKs) are detected prenatally, yet there is no clear consensus on initial evaluation and follow-up. We report the case of a 4-year-old male diagnosed with right pyelocalyceal dilation in utero, confirmed postnatally as MCDK. Follow-up ultrasounds revealed rapid growth of three upper pole cysts, reaching 8 cm.
View Article and Find Full Text PDFGynecol Oncol Rep
April 2025
Department of Pathology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Introduction: Ganglioglioma of the ovary is a rare neuroectodermal-type tumor, morphologically like its counterparts in the central nervous system, and only two cases have been reported before.
Case Report: The patient, a 30-year-old woman with no prior medical history of brain tumors or neurological disorders, was found to have a cystic mass in the left ovary, accompanied by two mural nodules. Histologically, the mural nodule in the teratoma exhibited a combination of neoplastic ganglion and glial cells.
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