| Literature DB >> 32028907 |
Rui Sun1, Hongwei Guan1, Hui Li2, Yixuan Bai1, Fei Wang3, Changzhong Li1.
Abstract
BACKGROUND: Uterine angioleiomyoma is a rare variant of leiomyoma, and the main therapy is complete surgery. This study introduces the benefit of three-dimensional computed tomography reconstruction for preoperative preparation. CASEEntities:
Keywords: Intravenous leiomyomatosis; Surgery; Three-dimensional CT reconstruction; Uterine angioleiomyoma; Volume rendering reconstructions
Mesh:
Year: 2020 PMID: 32028907 PMCID: PMC7006090 DOI: 10.1186/s12880-020-0417-2
Source DB: PubMed Journal: BMC Med Imaging ISSN: 1471-2342 Impact factor: 1.930
Fig. 1Axial slice of the CT image shows the shape and route of extension of the intravenous leiomyomatosis. a This image shows that the tumour grew into the right atrium and extended to the right ventricle; b This image shows that the tumour grew along the inferior vena cava, resulting in enlargement of the vein; c These two images show that the bilateral renal veins were not invaded; d This image shows that the leiomyoma grew into the vein through the right uterine vein and internal iliac vein
Fig. 2Sagittal and coronal slices of the CT multiplanar reformation show almost the whole appearance and travel path of the tumour; there was a continuous mass coursing through the inferior vena cava to the heart
Fig. 3A three-dimensional reconstruction image using the VR technique clearly shows the overall appearance of the tumour, the extent of invasion, the location of the tumour invading the blood vessel, the starting and ending location, the travel path, and the tumour dissemination. (The arrows point to the tumour inside (left) and behind (right) the uterus, and the purple tissue is the tumour growing inside the venous system)
Fig. 4The final shape of the tumour and the relationship between the tumour and the circulatory system
Fig. 5Microscopic picture of the patient. The tumour consisted of spindle cells (a), which encircled the blood vessels as they grew (b). Immunohistochemically, the tumour was positive for Desmin (c) and SMA (d), confirming its myogenic origin. It was negative for p53. The Ki-67 level was approximately 1%, indicating low cell division activity. The final diagnosis was IVL