ABSTRACT
Secondary abdominal pregnancy is a rare type of ectopic pregnancy. Following fertilization, the blastocyst escapes from the uterine cavity and implants in the peritoneal cavity. The early antenatal diagnosis and identification of the site and extent of placental implantation in an abdominal pregnancy are important to prepare for the eventual surgery. We present the case of a 24-year-old patient presenting with loss of fetal movement at 26 weeks of gestation for whom an abdominal pregnancy was suspected on ultrasonography and later confirmed on magnetic resonance imaging (MRI). She had one caesarean section in the past. The MRI findings suggested a scar dehiscence. She was eventually managed surgically, and the unviable fetus was removed. Abdominal pregnancies must be treated as emergencies. They usually present with complications such as fetal death and intra-abdominal hemorrhaging and can be easily missed on routine antenatal ultrasonography. The exact anatomical relationships of the fetus, the placenta, and vital maternal intra-abdominal structures can be accurately delineated with MRI, which greatly aids the management of patients with abdominal pregnancy. A proposed imaging protocol and technical suggestions for improving the diagnostic capability of ultrasonography and MRI in abdominal pregnancies have been provided to aid in the appropriate evaluation of suspect cases.
Subject(s)
Cesarean Section/adverse effects , Echo-Planar Imaging/methods , Pregnancy, Abdominal/diagnosis , Pregnancy, Abdominal/surgery , Prenatal Diagnosis/methods , Abortion, Therapeutic/methods , Emergencies , Female , Follow-Up Studies , Gestational Age , Humans , Laparotomy/methods , Pregnancy , Pregnancy, Ectopic/diagnostic imaging , Pregnancy, Ectopic/surgery , Preoperative Care/methods , Rare Diseases , Treatment Outcome , Ultrasonography, Prenatal/methods , Young AdultABSTRACT
Isomerism or Heterotaxy syndromes are rare multifaceted congenital anomalies with multi-system involvement. Grouped under the broad category of Situs Ambiguous defects, these often pose diagnostic difficulties due to their varied and confusing anatomy. Since patients rarely survive into adulthood due to cardiovascular complications, the etiology and natural history of such conditions are not fully understood. Imaging provides the most accurate non invasive method for diagnosis and thereby, prognosis in such cases. We present a case of right sided Isomerism with complex cardiac anomalies in a 17 year old adolescent, who presented with dysphagia as one of the main complaints. Multi modality imaging demonstrated the intricate abnormalities in vital systems.
Subject(s)
Abnormalities, Multiple/diagnosis , Heart Defects, Congenital/diagnosis , Adolescent , Deglutition Disorders/etiology , Dextrocardia/diagnosis , Diagnostic Imaging , Esophageal Stenosis/diagnosis , Heart Defects, Congenital/complications , Heterotaxy Syndrome/diagnosis , Humans , Liver/abnormalities , Male , Portal Vein/abnormalitiesABSTRACT
Accessory parotid glands are a common clinical occurrence and usually drain into the main Stenson's duct by small ductules and thereby, into the buccal cavity. Presence of an accessory parotid gland with an ectopic fistulous duct is a rare occurrence. We present the imaging findings in a case of right accessory parotid gland with ectopic fistulous duct associated with bilateral pre-aural appendages. Diagnostic workup was done by ultrasonography, sono-fistulography, contrast digital fistulography, contrast digital sialography and computed tomography fistulography. Imaging showed a right accessory parotid gland lying anterior to and separate from the main parotid gland draining via an ectopic fistulous duct opening over the right cheek. The child was managed surgically by internalisation of the duct to open into the buccal mucosa and excision of pre-aural appendages.
