| Literature DB >> 35979134 |
Abstract
BACKGROUND: Liver metastasis of duodenal gastrointestinal stromal tumor (GIST) is rare. Most reports mainly focus on its treatment and approaches to surgical resection, while details on its contrast-enhanced ultrasound (CEUS) findings are lacking. The diagnosis and imaging modalities for this condition remain challenging. CASEEntities:
Keywords: Case report; Contrast-enhanced ultrasound; Duodenal gastrointestinal stromal tumor; High frame rate; Metastatic liver cancer
Year: 2022 PMID: 35979134 PMCID: PMC9258392 DOI: 10.12998/wjcc.v10.i17.5899
Source DB: PubMed Journal: World J Clin Cases ISSN: 2307-8960 Impact factor: 1.534
Figure 1Magnetic resonance imaging findings. The lesion is approximately 2.3 cm in the left external lobe. A: T1-weighted image of the nodule showing hypo-intensity; B T2-weighted image of the tumor showing higher intensity; C: Diffusion-weighted image of the tumor showing a higher intensity; D: The lesion presented edge enhancement after reinforcement (white arrows).
Figure 2High-frame-rate contrast-enhanced ultrasound findings. Images showing high-frame-rate contrast-enhanced ultrasound perfusion patterns corresponding to those in contrast-enhanced ultrasound images. Concentric enhancement was more obvious. Irregular vessel column and rim enhancement can be seen (white arrows). A: Conventional ultrasound showing an uneven hypo-echo lesion with an approximate size of 3.5 cm × 2.2 cm × 2.4 cm and a peripheral hypoechoic halo located in the left lobe of the liver; B: Color Doppler flow imaging showing the dot-linear blood flow signal within the lesion; C-E: Contrast-enhanced ultrasound findings; F: The lesion showed heterogeneous hyper-enhancement at peak; G-J: We could not find obvious concentric and rim enhancement on contrast-enhanced ultrasound.
Figure 3Contrast-enhanced ultrasound quantitative analysis results. A-C: Contrast-enhanced ultrasound quantitative analysis showed ΔPI of 3.58 dB at peak; D-F: High-frame-rate contrast-enhanced ultrasound quantitative analysis showed ΔPI of 6.63 dB at peak.
Figure 4Histopathology findings. A: Microscopy showed a patchy distribution of short and spindle cells (H&E staining, × 200); B-D: Immunohistochemical staining displayed CD117 (+), Dog-1 (+), and Vimentin (+) (H&E staining, × 200).
Figure 5DNA sequencing electropherograms. DNA sequencing electropherograms revealed c-Kit 11 (c.1655_1699del 15 type), c-Kit 9, c-Kit 13, c-Kit 17, PDGFRα12, and PDGFRα18 wild type mutations.
Case and literature reports of patients with MLC sonographic features
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| Zhou J | China | 33/F | Increase in calcitonin and CEA | MTC | Hyper-and net-like; echogenicity, clear margin, well-defined shape | Hyper-enhancement during the arterial phase and hypo-enhancement in portal and parenchyma phase | Sonovue 1.2 mL | Surgery | Calcitonin and CEA remained normal |
| Corvino | Italy | 41/M | No specific symptoms | Rectal melanoma | Solitary hypo-anechoic complex cystic lesion with a thin internal septum | Hyper-enhancement of the cystic wall and intra-cystic septation during the arterial phase, rapid wash-out, and hypo-enhancement during the portal and late phases | Sonovue 2.4 mL | Surgery | N/A |
| Toni | Germany | 36/M | No specific symptoms | Choroidal melanoma | Iso-echogenicity | Homogeneous hyper-enhancement in arterial phase; hypo-enhancement in portal phase and punched-out enhancement defect; in late phase | Sonovue 2.0 mL | Surgery | N/A |
| Paulatto | France | 74/M | N/A | NOS of colon | N/A | Central part remains hypoechoic | N/A | Surgery | N/A |
| Ishikawa | Japan | N/A | N/A | Pancreas | Round with irregular margin | Strong peripheral enhancement in the arterial phase, early washout, hypo-enhancement in the portal, and post-vascular phases | Sonazoid 0.015 mL/kg | N/A | N/A |
| Michima | Japan | N/A | N/A | Breast | Clearly round, oval, or lobulated solid focal lesions, irregular margin. | Hypoechoic defects in enhancing parenchyma in the portal venous or postvascular phase | Sonazoid 0.015 mL/kg | N/A | N/A |
| Yang DP | China | N/A | N/A | Colorectum | Hypo- or mix- echogenicity and anechoic area | Capsule enhancement, starting time of washout of > 40 s, un-enhancement area, and proportion of non-enhancement area > 50% | Sonovue 2.4 mL | N/A | N/A |
| Wu | China | N/A | N/A | Colorectum | Not mentioned | Peripheral nodular enhancement, heterogeneous hyper-enhancement, or rim-like enhancement during the arterial phase and a non-enhancement area during the late phase | Sonovue 2.0 mL | N/A | N/A |
| Schwarze | Germany | N/A | N/A | NET of ileum | Anechoic oval-shaped | Earlier wash-in, hyperenhancement during the arterial phase, and hypo-enhancement in the portal phase | Not mentioned | N/A | N/A |
| Schwarze | Germany | N/A | N/A | Pancreas | N/A | Earlier wash-in, hyperenhancement during the arterial phase, and hypo-enhancement during the portal phase | Not mentioned | N/A | N/A |
| Zhang GD | China | N/A | N/A | Stomach | Round with regular margin, iso-echo | Earlier rim-like enhancement and washed out in portal phase, non-enhancement in late phase | Sonovue 2.4 mL | N/A | N/A |
| Zhang GD | China | N/A | N/A | Lung | Oval and hypo-echo | No significant enhancement, hypo-perfusion compared with liver parenchyma | Sonovue 2.4 mL | N/A | N/A |
F: Female; M: Male; MTC: Medullary thyroid cancer; CEA: Carcinoembryonic antigen; NOS: Non-otherwise specified; NET: Neuroendocrine tumor; N/A: Not available.