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Excision of extensive metastatic dysgerminoma to control refractory hypercalcaemia in a child at high risk for tumour-lysis syndrome

W Jawaid, V Solari, L Howell… - Journal of Pediatric Surgery, 2011 - Elsevier
Hypercalcaemia is a rare life-threatening complication of paediatric cancer that is commoner
in haematological than solid malignancies and associated rarely with acute renal failure. Often
refractory to medical therapy, control of hypercalcaemia in children with solid tumours ...
Cited by 1 - Related articles - All 3 versions

Is surgical restaging indicated in apparent stage IA pure ovarian dysgerminoma? The MITO group retrospective experience

G Mangili, C Sigismondi, D Lorusso, G Cormio… - Gynecologic …, 2011 - Elsevier
Overall recurrence rate was 11.5%: all recurrences occurred in the group submitted to incomplete
staging procedure. No patients treated with adjuvant chemotherapy relapsed. One patient had
pelvic recurrence, one patient relapsed in the abdomino-pelvic peritoneum and lymph ...
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[HTML] Ovarian dysgerminoma associated with pregnancy

[HTML] from koreamed.orgYK Lee, CY Yoo, G Lee… - Korean Journal of …, 2011 - synapse.koreamed.org
This is an Open Access article distributed under the terms of the Creative Commons Attribution
Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original ...
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Ovarian Dysgerminoma Associated With Fibrosarcoma: A Case Report

I Alvarado-Cabrero, R Valencia-Cedillo… - International Journal …, 2011 - journals.lww.com
A 35-year-old woman presented with abdominal pain and weight loss. Pelvic computed tomography
showed a 15 cm mass in the left ovary. Grossly, the removed ovary was completely replaced
by a solid tumor mass. On histological analysis (100 sections), the lesion showed the ...

Coexistence of gonadoblastoma and dysgerminoma in a dysgenetic gonad on touch preparation: A case report

Z Maleki, M Loveless… - Diagnostic Cytopathology, 2011 - Wiley Online Library
Swyer syndrome is known as pure gonadal dysgenesis. Individuals with Swyer syndrome are
phenotypically female with unambiguously female genital appearance at birth, and normal Mullerian
structures. The condition usually first becomes apparent in adolescence with delayed ...
Related articles - All 2 versions

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