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Dergiler / İstanbul Kuzey Klinikleri / 2022 / Cilt: 9 - Sayı: 1

Pseudo-Meigs syndrome secondary to endodermal sinus tumor

Ahmet Gökhan GÜLER
Can ACIPAYAM
Ali Erdal KARAKAYA
Dilan ALTINTAŞ URAL
Mehmet Cihan KARACAOĞLU
Sezen KOÇARSLAN
Mustafa Sabih KAYA
Sayfa
82–85
Yayın Tarihi
2022-10-18
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

This case is one of the rare cases presenting with Pseudo-Meigs syndrome and pathologically diagnosed as yolk sac tumor.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Ovarian tumors are the most common gynecological tumors seen in girls.
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Temel Bulgular & Veri:Approximately 60–70% of them are germ cell tumors.
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Sonuç & Katkı:This case is one of the rare cases presenting with Pseudo-Meigs syndrome and pathologically diagnosed as yolk sac tumor.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Ovarian tumors are the most common gynecological tumors seen in girls. Approximately 60–70% of them are germ cell tumors. Pseudo-Meigs syndrome is characterized by the presence of pelvic tumoral mass (benign or malign), pleural effusion, and massive acid. If the tumor is removed, acid and hydrothorax disappear. Endodermal sinus (yolk sac) tumor is a very rare cause in the diagnosis of Pseudo-Meigs syndrome, and only a few cases have been reported. This case is one of the rare cases presenting with Pseudo-Meigs syndrome and pathologically diagnosed as yolk sac tumor.

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Bu Makaleye Atıf Yap

GÜLER, A. G., ACIPAYAM, C., KARAKAYA, A. E., URAL, D. A., KARACAOĞLU, M. C., KOÇARSLAN, S., KAYA, M. S. (2022). Pseudo-Meigs syndrome secondary to endodermal sinus tumor. İstanbul Kuzey Klinikleri, Cilt: 9 - Sayı: 1, 82–85. https://ajindex.com/articles/551229

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Kaynakça (10)

  1. Cass DL, Hawkins E, Brandt ML, Chintagumpala M, Bloss RS, Milewicz AL, et al. Surgery for ovarian masses in infants, children, and adolescents: 102 consecutive patients treated in a 15-year period. J Pediatr Surg 2001;36:693–9
  2. Hayes-Jordan A. Surgical management of the incidentally identified ovarian mass. Semin Pediatr Surg 2005;14:106–10
  3. Shanbhogue AK, Shanbhogue DK, Prasad SR, Surabhi VR, Fasih N, Menias CO. Clinical syndromes associated with ovarian neoplasms: a comprehensive review. Radiographics 2010;30:903–19
  4. Jung NH, Kim T, Kim HJ, Lee KW, Lee NW, Lee ES. Ovarian sclerosing stromal tumor presenting as Meigs’ syndrome with elevated CA-125. J Obstet Gynaecol Res 2006;32:619–22
  5. Allmen DV. Ovarian tumors. In: Coran A, Caldamone A, Adzick, NS, Kurummel MT, Laberge MJ, Shamberger R, editors. Pediatric Surgery. Philadelphia: WB Saunders; 2012. p. 529–48
  6. Bridgewater JA, Rustin GJ. Pseudo-Meigs’ syndrome secondary to an ovarian germ cell tumor. Gynecol Oncol 1997;66:539–41
  7. Skiadas VT, Koutoulidis V, Eleytheriades M, Gouliamos A, Moulopoulos LA, Deligeoroglou E, et al. Ovarian masses in young adolescents: imaging findings with surgical confirmation. Eur J Gynaecol Oncol 2004;25:201–6
  8. Terauchi F, Onodera T, Nagashima T, Kobayashi Y, Moritake T, Oharaseki T, et al. Sclerosing stromal tumor of the ovary with elevated CA125. J Obstet Gynaecol Res 2005;31:432–5
  9. Amies Oelschlager AM, Gow KW, Morse CB, Lara-Torre E. Management of large ovarian neoplasms in pediatric and adolescent females. J Pediatr Adolesc Gynecol 2016;29:88–94
  10. Oltmann SC, Garcia N, Barber R, Huang R, Hicks B, Fischer A. Can we preoperatively risk stratify ovarian masses for malignancy? J Pediatr Surg 2010;45:130–4.