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异位和副脾病变的谱系。

Spectrum of Heterotopic and Ectopic Splenic Conditions.

机构信息

From the Department of Radiology, University of Wisconsin School of Medicine and Public Health, E3/311 Clinical Science Center, 600 Highland Ave, Madison, WI 53792-3252 (L.W.N., M.G.L., P.J.P.); Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, Mo (S.M.B., S.B.); and American College of Radiology (ACR) Institute for Radiologic Pathology (AIRP), Silver Spring, Md (M.G.L., P.J.P.).

出版信息

Radiographics. 2024 Nov;44(11):e240004. doi: 10.1148/rg.240004.

DOI:10.1148/rg.240004
PMID:39388371
Abstract

A spectrum of heterotopic and ectopic splenic conditions may be encountered in clinical practice as incidental asymptomatic detection or symptomatic diagnosis. The radiologist needs to be aware of these conditions and their imaging characteristics to provide a prompt correct diagnosis and avoid misdiagnosis as neoplasm or lymphadenopathy. Having a strong knowledge base of the embryologic development of the spleen improves understanding of the pathophysiologic basis of these conditions. Spleen-specific imaging techniques-such as technetium 99m (Tc)-labeled denatured erythrocyte scintigraphy, Tc-sulfur colloid liver-spleen scintigraphy, and MRI with ferumoxytol intravenous contrast material-can also be used to confirm the presence or absence of splenic tissue. Heterotopic splenic conditions include splenules and splenogonadal fusion (discontinuous or continuous forms). These heterotopic conditions are caused by incomplete fusion of the splenic primordia (splenule) and abnormal fusion of the gonadal and splenic tissue (splenogonadal fusion). Ectopic splenic conditions arise in patients with a prior splenic injury (splenosis), laxity or maldevelopment of the splenic ligaments (wandering spleen), or heterotaxy syndromes (polysplenia and asplenia). Importantly, these heterotopic and ectopic splenic conditions can also manifest with complications, including vascular torsion and rupture. RSNA, 2024.

摘要

在临床实践中,可能会偶然发现无症状的或有症状的各种异位和副脾情况。放射科医生需要了解这些情况及其影像学特征,以便能够迅速准确地做出诊断,避免误诊为肿瘤或淋巴结病。深入了解脾脏的胚胎发育有助于理解这些情况的病理生理基础。脾脏特异性成像技术,如锝 99m(Tc)标记变性红细胞闪烁扫描、Tc 硫胶体肝脾闪烁扫描和使用铁载氧体的 MRI,也可用于确认是否存在脾组织。异位脾情况包括脾小结和脾性腺融合(连续或不连续形式)。这些异位情况是由于脾原基(脾小结)融合不完全和性腺与脾组织异常融合(脾性腺融合)所致。脾副脾发生于脾损伤(脾种植)、脾韧带松弛或发育不良(游走脾)或异位轴综合征(多脾和无脾)的患者中。重要的是,这些异位和副脾情况也可能出现并发症,包括血管扭转和破裂。RSNA,2024。

相似文献

1
Spectrum of Heterotopic and Ectopic Splenic Conditions.异位和副脾病变的谱系。
Radiographics. 2024 Nov;44(11):e240004. doi: 10.1148/rg.240004.
2
The spleen: development and functional evaluation.脾脏:发育与功能评估。
Semin Nucl Med. 1985 Jul;15(3):276-98. doi: 10.1016/s0001-2998(85)80005-2.
3
[CT anatomy of the normal spleen: variants and pitfalls].
J Radiol. 2007 Apr;88(4):549-58. doi: 10.1016/s0221-0363(07)89854-4.
4
The value of combined 99mTc-Sn-colloid and 99mTc-RBC scintigraphy in the evaluation of a wandering spleen.
Ann Nucl Med. 1995 Aug;9(3):145-7. doi: 10.1007/BF03165042.
5
Clinical studies with spleen-specific radiolabeled agents.使用脾脏特异性放射性标记剂的临床研究。
Semin Nucl Med. 1985 Jul;15(3):260-75. doi: 10.1016/s0001-2998(85)80004-0.
6
Mass at the splenic hilum: a clue to torsion of a wandering spleen located in a normal left upper quadrant position.脾门处肿物:位于正常左上腹位置的游走脾扭转的线索。
J Ultrasound Med. 2003 May;22(5):527-30. doi: 10.7863/jum.2003.22.5.527.
7
Multimodality imaging of developmental splenic anomalies: tips and pitfalls.发育性脾异常的多模态影像学:技巧与陷阱。
Clin Radiol. 2022 May;77(5):319-325. doi: 10.1016/j.crad.2021.12.014. Epub 2022 Jan 7.
8
Intrathoracic splenosis: evaluation by superparamagnetic iron oxide-enhanced magnetic resonance imaging and radionuclide scintigraphy.胸腔内脾组织转移:超顺磁性氧化铁增强磁共振成像与放射性核素闪烁扫描评估。
Jpn J Radiol. 2009 Nov;27(9):371-4. doi: 10.1007/s11604-009-0350-3. Epub 2009 Nov 27.
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Anatomic and functional asplenia--absence of the splenic image during 99mTc-sulfur colloid scintigraphy.
Semin Nucl Med. 1982 Jan;12(1):95-6. doi: 10.1016/s0001-2998(82)80033-0.
10
A simplified method of selective spleen scintigraphy with Tc-99m-labeled erythrocytes: clinical applications. Concise communication.
J Nucl Med. 1980 May;21(5):413-6.

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