Mediastinal mature teratoma with coexistence of angiosarcoma, granulocytic sarcoma and a hematopoietic region in the tumor: A rare case of association between hematological malignancy and mediastinal germ cell tumor

1998 ◽  
Vol 48 (9) ◽  
pp. 749-753 ◽  
Author(s):  
Atsuko Saito ◽  
Kazuo Watanabe ◽  
Takashi Kusakabe ◽  
Masafumi Abe ◽  
Toshimitsu Suzuki
2005 ◽  
Vol 101 (1) ◽  
pp. 159-161 ◽  
Author(s):  
Spilios M. Karas ◽  
John T. Parissis ◽  
Charalambos Antoniades ◽  
Achilleas Loulias

2019 ◽  
Vol 12 (4) ◽  
pp. 228-229
Author(s):  
Sarbajit Mukherjee ◽  
Sami Ibrahimi ◽  
Teresa Scordino ◽  
Mohamad Cherry

2021 ◽  
Vol 9 ◽  
Author(s):  
Ruslan Bilal ◽  
Dastan Rustemov ◽  
Zhenis Sakuov ◽  
Bahytkaly Ibraimov ◽  
Arman Kozhakhmetov

Omphalocele is a congenital malformation of the abdominal wall, which occurs with a frequency of 1–5,000 newborns. The prognosis of treatment often depends on the presence of concomitant malformations. The most common contents of the hernia with omphalocele are the intestinal loops, liver, spleen. However, all organs of the abdominal cavity can be part of the hernial sac with large sizes of omphalocele. Teratoma is a germ cell tumor made up of several different types of tissue, such as hair, muscle, teeth, or bone. They are a type of germ cell tumor and divided into two types: mature and immature. In this article, we describe a rare case of a combination of an omphalocele with a mature teratoma and report the successful single step surgical treatment. On the first day after birth, a simultaneous operation—Removal of teratoma with abdominoplasty was performed. The postoperative period was uneventful, and the child was discharged for recovery.


2020 ◽  
Vol 22 (Supplement_3) ◽  
pp. iii329-iii329
Author(s):  
Hiroki Yamada ◽  
Tomohiro Abiko ◽  
Hirokazu Fujiwara ◽  
Kazunari Yoshida ◽  
Hikaru Sasaki

Abstract INTRODUCTION Germ cell tumors in the central nervous system (CNS) typically arise either at suprasellar and/or pineal region, and occasionally at basal ganglia. We report a case of diagnostically challenging, recurrent germ cell tumor presented with diffuse intraaxial abnormality in and across the lower brainstem, which was diagnosed by the elevated placental alkaline phosphatase (PLAP) level in cerebrospinal fluid (CSF). CASE DESCRIPTION: A 28-year-old man had been treated by chemoradiotherapy at the previous hospital for bifocal suprasellar and pineal lesions with the provisional diagnosis of germinoma without histological confirmation. Three years later, he presented with progressive weakness of bilateral extremities for weeks. Magnetic resonance imaging showed a diffuse, bilaterally symmetric high intensity lesion on T2-weighted image with slight contrast enhancement across the ventral side of the medulla oblongata to the upper cervical spinal cord. Serum and CSF hCG, hCG-β, and AFP were all negative. Since the image findings were atypical for recurrent germ cell tumor, some kind of myelitis was initially suspected. Therefore, steroid pulse therapy was administered. However, the patient’s symptom was still gradually progressing. Then, the CSF PLAP turned out to be positive, indicating the recurrence of germinoma. Accordingly, platinum-based chemotherapy was administered, and the imaging findings, patient’s symptoms, and CSF PLAP began to improve. The patient is to be treated with radiotherapy following chemotherapy. CONCLUSION We report a rare case of CNS germ cell tumor that presented with diffuse intraaxial lesion in the lower brainstem in which examination of CSF PLAP was extremely useful.


2020 ◽  
Author(s):  
Paolo Pedrazzoli ◽  
David Rondonotti ◽  
Carlo Cattrini ◽  
Simona Secondino ◽  
Paolo Ravanini ◽  
...  

1992 ◽  
Vol 61 (1) ◽  
pp. 67-73 ◽  
Author(s):  
Willem E. de Graaff ◽  
J. Wolter Oosterhuis ◽  
Bauke de Jong ◽  
Jannie van Echten-Arends ◽  
Janneke Wiersema-Buist ◽  
...  

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