Anda belum login :: 27 Nov 2024 06:59 WIB
Detail
ArtikelOvarian preservation in a young patient with Gorlin syndrome and multiple bilateral ovarian masses  
Oleh: Morse, Christopher B. ; McLaren, Janet F. ; Roy, Darshan ; Siegelman, Evan S.
Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Fertility and Sterility (keterangan: ada di ClinicalKey) vol. 96 no. 01 (Jul. 2011), page e47-e50.
Topik: Gorlin syndrome; nevoid basal cell carcinoma syndrome; fertility preservation; ovarian conservation; preimplantation genetic diagnosis
Ketersediaan
  • Perpustakaan FK
    • Nomor Panggil: F02.K.2011.04
    • Non-tandon: 1 (dapat dipinjam: 0)
    • Tandon: tidak ada
    Lihat Detail Induk
Isi artikelObjective To report a case of bilateral ovarian fibromas and ovarian leiomyomas in a young patient with Gorlin syndrome and to highlight issues of fertility preservation, ovarian conservation, and preimplantation genetic diagnosis in this population. Design Case report. Setting University hospital. Patient(s) A 15-year-old female patient with Gorlin syndrome and bilateral ovarian masses. Intervention(s) Ultrasound, magnetic resonance imaging, hormone analysis, and laparotomy with resection of ovarian fibromas. Main Outcome Measure(s) Preservation of ovarian function, pathologic diagnosis. Result(s) Our patient represented an adolescent case of bilateral ovarian fibromas and leiomyomas in Gorlin syndrome presenting with menstrual irregularities. She was managed surgically with resection of the lesions and conservation of normal ovarian tissue. Conclusion(s) In Gorlin syndrome, ovarian fibromas are a common clinical manifestation. Patients with ovarian involvement may present with complex gynecologic needs and may have decreased fertility potential. Careful surgical management, follow-up, and counseling on options for future fertility should be offered to all patients.
Opini AndaKlik untuk menuliskan opini Anda tentang koleksi ini!

Kembali
design
 
Process time: 0.015625 second(s)