TY - JOUR
T1 - Posterior fossa ring-enhancing lesions in the adult immunocompetent host
T2 - illustrative cases, systematic review, and proposed diagnostic algorithm
AU - Van Boxstael, Elisabeth
AU - de Hennin, Alexia
AU - Vigneul, Eric
AU - Scoppettuolo, Pasquale
AU - El Sankari, Souraya
AU - Bocchio, Anna Paola
AU - Borrelli, Serena
AU - Lolli, Valentina
AU - van Pesch, Vincent
AU - Slootjes, Sofia Maldonado
AU - Finet, Patrice
AU - Rovira, Àlex
AU - Reich, Daniel S
AU - Maggi, Pietro
N1 - © 2025 by American Journal of Neuroradiology.
PY - 2025/8/1
Y1 - 2025/8/1
N2 - PURPOSE: Posterior fossa ring-enhancing lesions (PFREL) in the adult immunocompetent hosts pose a diagnostic challenge. We aimed to evaluate the spectrum of PFREL etiologies and propose a diagnostic algorithm.METHODS: This study involved a retrospective analysis of PFREL cases from our institution (January 2023 to April 2024) and a systematic literature review conducted using Embase and PubMed databases following the PRISMA 2020 guidelines. Clinical and radiological features from these cases formed the basis of a diagnostic algorithm, which was further refined via an additional comprehensive literature review, and finally validated on an independent set of PFREL cases.RESULTS: The systematic review (467 studies, 56 selected after inclusion/exclusion criteria) revealed that PFREL etiology was infectious in 52%, tumoral in 38% and inflammatory in 2% of cases. At initial presentation, mean age was 48 years and 36% of patients had multiple PFREL. Headache was the most common symptom (46%). Among those with reported outcomes, 36% showed complete resolution of symptoms, 29% showed improvement with residual symptoms, and 16% died. The diagnostic algorithm was created from a total of 116 PFREL cases (10 from our institutional series, 56 from the systematic literature review and 50 supplementary cases found in the literature) and included 29 possible PFREL etiologies. In the validation set (16 patients), the algorithm provided the correct diagnosis in each case.CONCLUSION: PFREL in immunocompetent adults encompass a broad differential diagnosis. Our algorithm integrates clinical and radiologic data to assist in identifying the underlying cause of PFREL, potentially reducing the need for neurosurgical biopsy. This approach aims to enhance diagnostic accuracy, leading to better treatment decisions and improved patient outcomes.ABBREVIATIONS: ADEM = acute disseminated encephalomyelitis; CLL = chronic lymphocytic leukemia; CSF = cerebrospinal fluid; DLBCL: diffuse large B cell lymphoma; FLAIR = fluid attenuated inversion recovery; MeSH = medical subject headings; MRI = magnetic resonance imaging; NIHSS = National Institutes of Health Stroke Scale; NMOSD = neuromyelitis optic spectrum disorder; PFREL = posterior fossa ring enhancing lesion; PRISMA = Preferred Reporting Items for Systematic reviews and Meta-Analyses; SUV max = maximum standardized uptake value.
AB - PURPOSE: Posterior fossa ring-enhancing lesions (PFREL) in the adult immunocompetent hosts pose a diagnostic challenge. We aimed to evaluate the spectrum of PFREL etiologies and propose a diagnostic algorithm.METHODS: This study involved a retrospective analysis of PFREL cases from our institution (January 2023 to April 2024) and a systematic literature review conducted using Embase and PubMed databases following the PRISMA 2020 guidelines. Clinical and radiological features from these cases formed the basis of a diagnostic algorithm, which was further refined via an additional comprehensive literature review, and finally validated on an independent set of PFREL cases.RESULTS: The systematic review (467 studies, 56 selected after inclusion/exclusion criteria) revealed that PFREL etiology was infectious in 52%, tumoral in 38% and inflammatory in 2% of cases. At initial presentation, mean age was 48 years and 36% of patients had multiple PFREL. Headache was the most common symptom (46%). Among those with reported outcomes, 36% showed complete resolution of symptoms, 29% showed improvement with residual symptoms, and 16% died. The diagnostic algorithm was created from a total of 116 PFREL cases (10 from our institutional series, 56 from the systematic literature review and 50 supplementary cases found in the literature) and included 29 possible PFREL etiologies. In the validation set (16 patients), the algorithm provided the correct diagnosis in each case.CONCLUSION: PFREL in immunocompetent adults encompass a broad differential diagnosis. Our algorithm integrates clinical and radiologic data to assist in identifying the underlying cause of PFREL, potentially reducing the need for neurosurgical biopsy. This approach aims to enhance diagnostic accuracy, leading to better treatment decisions and improved patient outcomes.ABBREVIATIONS: ADEM = acute disseminated encephalomyelitis; CLL = chronic lymphocytic leukemia; CSF = cerebrospinal fluid; DLBCL: diffuse large B cell lymphoma; FLAIR = fluid attenuated inversion recovery; MeSH = medical subject headings; MRI = magnetic resonance imaging; NIHSS = National Institutes of Health Stroke Scale; NMOSD = neuromyelitis optic spectrum disorder; PFREL = posterior fossa ring enhancing lesion; PRISMA = Preferred Reporting Items for Systematic reviews and Meta-Analyses; SUV max = maximum standardized uptake value.
UR - http://www.scopus.com/inward/record.url?scp=105012482852&partnerID=8YFLogxK
U2 - 10.3174/ajnr.A8677
DO - 10.3174/ajnr.A8677
M3 - Article
C2 - 39880690
SN - 0195-6108
VL - 46
SP - 1534
EP - 1541
JO - American Journal of Neuroradiology
JF - American Journal of Neuroradiology
IS - 8
M1 - ajnr.A8677
ER -