2023
DOI: 10.3390/diagnostics13152536
|View full text |Cite
|
Sign up to set email alerts
|

Incidental Focal Spleen Lesions: Integrated Imaging and Pattern Recognition Approach to the Differential Diagnosis

Antonio Corvino,
Vincenza Granata,
Domenico Tafuri
et al.

Abstract: Spleen lesions and pseudolesions, detected incidentally in imaging, are not uncommon and may require further work-up. The imaging appearance of focal splenic lesions (FSLs) may not be pathognomonic, because of considerably overlapping features. Consequently, all imaging techniques lack specificity to fully characterize FSLs. Clinical correlation is mandatory, so as, first of all, to categorize the patient as having or not having a history of solid or hematologic malignancy. Nowadays, many patients have old ima… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
2
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
9

Relationship

3
6

Authors

Journals

citations
Cited by 9 publications
(5 citation statements)
references
References 48 publications
0
2
0
Order By: Relevance
“…GISTs are rare tumors originating from the interstitial cells of Cajal in the muscularis propria, although they are considered the most common mesenchymal tumor of the GI tract (incidence worldwide of 1-2 per 100,000). They arise from abnormal proliferation of interstitial cells of Cajal that are electrical pacemakers and mediators of enteric neurotransmission in the muscularis propria of the GI tract, with 95% of the tumors staining positive for CD117 (c-KIT) and 70% for CD34 [14], in most cases caused by oncogenic activating mutation of the receptor tyrosineproteinkinase [1][2][3]. Their incidence is very uncommon when compared to GI carcinoma [15] and they usually occur after 40 years of age, most commonly in older patients (median age 60-65 years) with a slight male predilection [9,10].…”
Section: Discussionmentioning
confidence: 99%
“…GISTs are rare tumors originating from the interstitial cells of Cajal in the muscularis propria, although they are considered the most common mesenchymal tumor of the GI tract (incidence worldwide of 1-2 per 100,000). They arise from abnormal proliferation of interstitial cells of Cajal that are electrical pacemakers and mediators of enteric neurotransmission in the muscularis propria of the GI tract, with 95% of the tumors staining positive for CD117 (c-KIT) and 70% for CD34 [14], in most cases caused by oncogenic activating mutation of the receptor tyrosineproteinkinase [1][2][3]. Their incidence is very uncommon when compared to GI carcinoma [15] and they usually occur after 40 years of age, most commonly in older patients (median age 60-65 years) with a slight male predilection [9,10].…”
Section: Discussionmentioning
confidence: 99%
“…In comparison with other methods, US can highlight small effusions <15 mL unlike chest x‐ray, which requires a minimum of 150 mL 33 . US is comparable to computed tomography (CT), even if CT itself has some limitations; indeed, it is a method compulsorily performed in the supine position, unlike US, and it is not able to optimally differentiate the consolidation portion from the liquid portion in cases where it is performed without a contrast medium 43–45 . Therefore, US is a method capable of early detecting the formation of a pleural effusion, which can be extremely useful in patients with suspected extension of neoplastic disease of the breast both in the primary form and as a relapse of the disease 46,47 …”
Section: Discussionmentioning
confidence: 99%
“…Early PLCH can have the same features as RB-ILD, presenting as bronchiolocentric ill-defined micronodules generally associated with mild centrilobular emphysema [32]. Differential diagnosis with GPA can be challenging due to the bronchiolocentric distribution of micronodules, often cavitated [102][103][104][105].…”
Section: Diagnosismentioning
confidence: 99%