A case report on rare co-occurrence of invasive ovarian mucinous adenocarcinoma, unilateral renal agenesis, and bicornuate uterus: is it a new triad?

被引:2
作者
Mbwambo, Orgeness Jasper [1 ,2 ]
Anthony, Jonaviva [1 ]
Mremi, Alex [3 ,4 ]
Ngowi, Nicholas B. [1 ,2 ]
Mvunta, David H. [5 ,6 ,7 ]
机构
[1] Kilimanjaro Christian Med Univ Coll KCMUCO, Dept Urol, POB 2240, Moshi, Tanzania
[2] Kilimanjaro Christian Med Ctr KCMC, Dept Urol, POB 3010, Moshi, Tanzania
[3] Kilimanjaro Christian Med Ctr KCMC, Dept Pathol, POB 3010, Moshi, Tanzania
[4] Kilimanjaro Christian Med Univ Coll KCMUCO, Dept Pathol, POB 2240, Moshi, Tanzania
[5] Ocean Rd Canc Inst ORCI, Dept Clin Oncol, Barack Obama Dr,POB 3592, Dar Es Salaam, Tanzania
[6] Muhimbili Univ Hlth & Allied Sci, Dept Obstet & Gynecol, 9 UN Rd,POB 65017, Dar Es Salaam, Tanzania
[7] St Joseph Coll Hlth & Allied Sci, Dept Obstet & Gynecol, POB 11007, Dar Es Salaam, Tanzania
关键词
Case report; Ovarian mucinous adenocarcinoma; Renal agenesis; Bicornuate uterus; CONGENITAL UTERINE ANOMALIES; PREVALENCE;
D O I
10.1186/s12905-024-03130-y
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Concomitant invasive ovarian mucinous adenocarcinoma, unilateral renal agenesis and bicornuate uterus is a rare combination. Unilateral renal agenesis has been associated with genital anomalies, such as unicornuate and bicornuate uterus. Furthermore, a wealth of studies has reported the association between unicornuate uterus and ovarian anomalies, such as the absence of an ovary or ectopic ovaries, but rarely has there been a combination of the three to the best of our knowledge. The present case report is the first case presentation with a combination of the three syndromes: ovarian mucinous tumor, unilateral renal agenesis, and bicornuate uterus.Case presentation We report the case of a 17-year-old who presented with abdominal distension. On examination, a CT scan revealed a large multicystic abdominal mass on the right side, with an absence of the right kidney while the left kidney was normal in size, appearance, and position. Intraoperatively, massive blood-stained ascitic fluid was evacuated. Additionally, a large whitish polycystic intra-abdominal mass with mucus-like materials and solid areas was attached to the midpoint of the colon and the right ovary, with visible metastasis to the omentum. The uterus was bicornuate. The mass and omentum were taken for histopathology and a diagnosis of invasive ovarian mucinous cystadenocarcinoma with metastasis to the colon and omentum was made after a pathological report.Conclusions The presence of these conditions in the same individual could potentially complicate medical management and fertility considerations. Thus, a need for a multidisciplinary medical team, including gynecologists, urologists, and oncologists, to address their unique needs and provide appropriate treatment and guidance. Further research and case studies are needed to better understand the possible association and implications of these rare co-occurring conditions.
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