A rare case of caudal regression syndrome in a foetus of non-diabetic mother : a case report

Backgound: Caudal regression syndrome (CRS) is an uncommon disorder in which there is abnormal development of the caudal end of the foetal spine along with many associated anomalies. Manifestations of this syndrome can vary from the absence of a few terminal coccygeal segments to complete lumbosacral agenesis. Its overall incidence is 1 in 60000 live births. It is more commonly seen in infants of diabetic mothers, with a 200-fold increased risk as compared to the general population. Case Report: We present a case of CRS in a foetus of a non-diabetic mother and discuss the role of radiology in early diagnosis and timely management. We also correlate initial abnormalities of the nervous system found on imaging with postnatal clinical deficits. Conclusions: This case highlights the rarity caudal regression syndrome in a foetus of a non-diabetic mother. Early diagnosis of CRS is important for appropriate management

A Rare Case of Huge Renal Leiomyosarcoma and Imaging Diagnostic Dilemma

Soft tissue sarcomas are rare mesenchymal tumours. Leiomyosarcoma is a rare malignant tumour of smooth muscle origin that generally arises from soft tissues and uterine tissue. On occasions, they may arise from smooth muscle of the vessel walls, more commonly from the veins. Renal leiomyosarcomas frequently originates from the smooth muscles of renal capsule, renal pelvis or renal vessels. Correct diagnosis and appropriate management is very essential in such cases. We highlight the possibility of malignant soft tissue sarcoma like leiomyosarcoma in the kidney. We emphasize on the suspicion of rare possibility and clinicopathological correlation is required to identify such cases, which has pronounced prognostic implications as whether to do surgical resection or biopsy or treat such patient with chemotherapy or radiotherapy vary with diagnosis