Results 11 to 20 of about 1,480 (145)

Primary Yolk Sac Tumor of the Endometrium: A Case Report and Comprehensive Literature Review. [PDF]

Case Rep Pathol
Yolk sac tumor (YST) of the endometrium is very rare, with fewer than 40 cases reported in the English literature. We here describe a case of primary endometrial YST and discuss the clinicopathological features with a literature review. A 66‐year‐old Chinese woman presented with abnormal vaginal bleeding for 15 days and a uterine mass for 3 days.
Cheng H, Song Y, Shi SS.
europepmc   +2 more sources

A Toddler With Iron Deficiency Anemia Secondary to a Yolk Sac Tumor of the Stomach: A Case Report and Literature Review. [PDF]

Case Rep Pediatr
Yolk sac tumors, a subset of malignant germ cell tumors originating from gonadal germ cells, most often present as ovarian or testicular tumors in adolescents, sometimes in combination with different types of histology as a mixed malignant germ cell tumor.
Saleem N, Sylvestre PB, Chien FL, Gonzalez RS, Vega JEV, Mitchell S.   +5 more
europepmc   +2 more sources

Endodermal sinus tumor of testis with acute intestinal obstruction: A rare presentation

Journal of Indian Association of Pediatric Surgeons, 2012
A 7-year-old boy reported with endodermal sinus tumor of left testis, jejunal metastasis and intestinal obstruction. He was treated by high inguinal orchidectomy and resection of jejunal mass followed by chemotherapy.
Biswanath Mukhopadhyay, Ram M Shukla, Madhumita Mukhopadhyay, Kartik Chandra Mandal, Dipankar Roy   +4 more
doaj   +2 more sources

A Rare Incidental Finding: Heterotopic Salivary Gland Tissue Adjacent to Dermatofibrosarcoma Protuberans of the Abdominal Wall. [PDF]

Case Rep Pathol
Summary: This case presents incidental heterotopic salivary gland tissue adjacent to a dermatofibrosarcoma protuberans (DFSP) located in the abdominal wall. The mature, functional heterotopic tissue was identified during Mohs micrographic surgery (MMS) performed for a DFSP, a slow‐growing cutaneous tumor with locally aggressive and potentially ...
Ángeles LB, Bustillos DKB, Vila JAC, Victoria TRT, Memije MEV, Niebla RML.   +5 more
europepmc   +2 more sources

Current Trends in the Surgical Management of Yolk Sac Tumors [PDF]

Current Oncology
Mediastinal yolk sac tumors (YST) constitute a highly malignant subtype of primary non-seminomatous germ cell tumors, which are often locally advanced and unresectable at diagnosis.
Małgorzata Edyta Wojtyś, Konstantinos Kostopanagiotou, Dawid Kordykiewicz, Patryk Skórka, Alexandros Polykarpos Gkioulekas, Julia Augusta Guimarães Dourado, Janusz Wójcik, Periklis Tomos   +7 more
doaj   +2 more sources

Yolk Sac Tumor of the Ovary in Mosaic 46XX Turner Syndrome [PDF]

International Journal of Women's Health
Alfonsus Zeus Suryawan, Dian Tjahyadi, Martin Hermawan, Doni Aprialdi Department of Obstetrics and Gynecology; Universitas Padjadjaran, Bandung, IndonesiaCorrespondence: Alfonsus Zeus Suryawan, Department of Obstetrics and Gynecology, Universitas ...
Suryawan AZ, Tjahyadi D, Hermawan M, Aprialdi D   +3 more
doaj   +2 more sources

A sinonasal yolk sac tumor in an adult [PDF]

Journal of Pathology and Translational Medicine, 2022
Yolk sac tumors (YSTs), which are also called endodermal sinus tumors, are malignant tumors of germ cell origin. These tumors usually occur in the gonads, but 20% of cases have been reported at extragonadal sites.
Jaehoon Shin, Ji Heui Kim, Kyeong Cheon Jung, Kyung-Ja Cho   +3 more
doaj   +1 more source

Anesthesia for mandibular yolk sac tumor in children after radiotherapy and chemotherapy: A case report

Clinical Case Reports, 2022
Yolk sac tumor (YST), also known as endodermal sinus tumor, is a malignant germ cell tumor that usually affects children aged >3 years. It is commonly observed in the gonadal sites (testis or ovary) but is extremely rare in the mandibular regions.
Shuiting Zhang, Liang Wen, Hui Zou, Shaosan Liu, Ruping Dai   +4 more
doaj   +1 more source

Endodermal sinus tumor of the pineal region [PDF]

Cancer, 1980
Two cases of endodermal sinus tumor of the pineal region are reported and compared with 16 others in the literature. The preponderance of neoplasms occurs in boys, usually in their second decade. The diagnosis is usually established within three months of the onset of non-specific symptoms of an intracranial mass.
D, Tavcar, S J, Robboy, P, Chapman
openaire   +2 more sources

Mediastinal endodermal sinus tumor associated with fatal hemophagocytic syndrome

Hematology/Oncology and Stem Cell Therapy, 2011
The association of endodermal sinus tumor, known also as yolk sac tumor, of the mediastinum with hemophagocytic syndrome is exceedingly rare with only a few cases on record. We report a 24-year-old male who had a large mediastinal germ cell tumor, proven
Ikram Ul Haq Chaudhary, Shoukat Ahmad Bojal, Adel Attia, Battal Al-Dossary, Afra Qasem Al Dayel, Samir Sami Amr   +5 more
doaj   +1 more source