Publikasi Scopus FKUI 2021 per tanggal 31 Mei 2021 (358 artikel)

Harzif A.K., Ambalagen S., Charilda F.E., Mutia H.D.
57191493435;57222325337;57222329284;57214329625;
A rare case of multiple leiomyomas on rudimentary uterus in a woman with Mayer Rokitansky Kuster Hauser (MRKH) syndrome: A challenging diagnosis and laparoscopic approach
2021
International Journal of Surgery Case Reports
81
105711
Division of Reproductive Immuno-Endocrinology, Department of Obstetrics and Gynecology, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital Jakarta, Indonesia; Department of Obstetrics and Gynecology, Dr. Cipto Mangunkusumo Hospital Jakarta, Faculty of Medicine Universitas Indonesia, Pangeran Diponegoro Street No. 71, Kenari, Jakarta, Indonesia; Indonesian Reproductive Medicine Research and Training Center (INA- REPROMED), Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital Jakarta, Pangeran Diponegoro Street No. 71, Kenari, Central of Jakarta, 10430, Indonesia
Harzif, A.K., Division of Reproductive Immuno-Endocrinology, Department of Obstetrics and Gynecology, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital Jakarta, Indonesia; Ambalagen, S., Department of Obstetrics and Gynecology, Dr. Cipto Mangunkusumo Hospital Jakarta, Faculty of Medicine Universitas Indonesia, Pangeran Diponegoro Street No. 71, Kenari, Jakarta, Indonesia; Charilda, F.E., Indonesian Reproductive Medicine Research and Training Center (INA- REPROMED), Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital Jakarta, Pangeran Diponegoro Street No. 71, Kenari, Central of Jakarta, 10430, Indonesia; Mutia, H.D., Indonesian Reproductive Medicine Research and Training Center (INA- REPROMED), Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo Hospital Jakarta, Pangeran Diponegoro Street No. 71, Kenari, Central of Jakarta, 10430, Indonesia
Mayer Rokitansky Kuster Hauser (MRKH) syndrome is a congenital disorder involving reproductive, genitourinary, bone, and cardiac malformation. The incidence is 1 in 4000–5000 females livebirths. The phenotype is female 46 XX karyotype, normal secondary sexual characteristics, and normal functional ovaries. The occurrence of leiomyoma in uterine remnant in MRKH syndrome is a very rare case, even though several cases have been reported. The diagnosis and management approach, in this case, is quite challenging. Here, we report a 38 years old female who represents multiple leiomyomas on the rudimentary uterus, then we did laparoscopic removal of the fibroids and adjacent rudimentary uterus. © 2021
Case report; Laparascopic; Mayer Rokitansky Kuster Hauser (MRKH) syndrome; Multiple leiomyomas; Rudimentary uterus
analgesic agent; abdominal discomfort; abdominal pain; adult; analgesia; Article; clinical assessment; echography; family history; female; genital system; hair; histopathology; human; infertility; karyotype 46,XX; laparoscopic surgery; leiomyoma; major clinical study; multiple cancer; nuclear magnetic resonance imaging; ovary function; pelvic examination; physical examination; primary amenorrhea; priority journal; Rokitansky syndrome; secondary sexual characteristics; sexual intercourse; transabdominal ultrasonography; transrectal ultrasonography; uterus horn; uterus myoma; vagina mucosa
Elsevier Ltd
22102612
Article
Q3
233
16893