Cargando…
A rare occurrence of psoas abscess with uterine didelphys and renal agenesis: A case report
INTRODUCTION: Mullerian duct anomaly such as uterine didelphys is a rare congenital anomaly of female genitourinary tract presenting with dysmenorrhea, hematocolpus, and subfertility in adolescent females. It is commonly associated with wolffian duct anomaly like renal agenesis. Here we present a ra...
Autores principales: | Mandal, Sujit Kumar, Shikhrakar, Shreeja, Regmi, Binit Upadhaya, Bam, Shiba |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429909/ https://www.ncbi.nlm.nih.gov/pubmed/34527237 http://dx.doi.org/10.1016/j.amsu.2021.102802 |
Ejemplares similares
-
Uterus didelphys with unilateral obstructed hemivagina with hematometrocolpos and hematosalpinx with ipsilateral renal agenesis
por: Jindal, Gaurav, et al.
Publicado: (2009) -
OHVIRA: Uterus didelphys, blind hemivagina and ipsilateral renal agenesis: Advantage MRI
por: Bajaj, Sunil K, et al.
Publicado: (2012) -
An Unusual Diagnosis of Sporadic Type III Osteogenesis Imperfecta in the First Day of Life
por: Shikhrakar, Shreeja, et al.
Publicado: (2022) -
Herpes simplex esophagitis in an immunocompetent host: a case report
por: Upadhaya Regmi, Binit, et al.
Publicado: (2021) -
Uterine Carcinosarcoma in a Patient with Didelphys Uterus
por: Iavazzo, C., et al.
Publicado: (2013)