Avoid common mistakes on your manuscript.
Case Report
A 68-year-old female was admitted to the emergency department due to headache, mental confusion and a mild hemiparesis on the left side in October 2021. Her medical history revealed dilatative cardiomyopathy, arterial hypertension and nicotine abuse but no known malignancy. Clinical evaluation yielded a hemiparesis on the left side grade 4 according to the Medical Research Council (MRC) scale. Magnetic resonance imaging (MRI) was performed and showed a right temporal mass lesion with perifocal edema. The case was discussed at the interdisciplinary neuro-oncological board and surgery was indicated.
At surgery a temporal craniotomy was performed followed by a temporal pole resection with resection of the temporomesial structures. The surgery was uneventful and the patient had no new neurological deficits. A postoperative MRI scan showed a complete resection of the contrast-enhancing portions. The patient was transferred to an oncology ward. Due to renal insufficiency, the chemotherapy could only be started with a reduced dose of cytarabine and without methotrexate. The chemotherapy was well tolerated. No tumour recurrence has been detected in the regular follow-up MRIs to date.
Imaging
The MRI showed a large space-occupying intra-axial lesion of the right temporal lobe (Figs. 1, 2 and 3). On the fluid-attenuated inversion recovery (FLAIR) images the lesion (Fig. 1, arrowhead) could hardly be discriminated from the extended perifocal edema (Fig. 1, arrow). On T1-weighted images after administration of gadolinium (Gd), the lesion showed distinct, giriform contrast enhancement (Fig. 2a–c, arrowheads) with signs of central necrosis (Fig. 2a, arrow). Note the large perifocal edema (Fig. 2b, c, arrow). On diffusion-weighted MRI (b-value: 1000) the lesion did not display any signs of restricted diffusion (not shown). On dynamic susceptibility-weighted, contrast-enhanced (DSC) perfusion MRI the lesion showed increased perfusion on the cerebral blood volume (CBV) map (Fig. 3a, arrows). The signal intensity-time curve (Fig. 3b), derived from a region of interest (ROI) within the CBV map, markedly exceeded the baseline after the first pass (Fig. 3b, red circle).
Differential Diagnosis
Glioblastoma
Glioblastomas (GBM, IDH wildtype) are the most common primary central nervous system (CNS) tumors in adults, mostly arising supratentorially with a preponderance in men in the 7th decade of life [1]. According to the recent World Health Organization (WHO) criteria they represent high-grade, rapidly growing, diffusely infiltrating astrocytic tumors, classified as CNS WHO grade 4 neoplasms, with a poor prognosis [2, 3]. Due to aggressive and rapid growth, glioblastomas usually show signs of neovascularization and necrosis, surrounded by diffuse tumor infiltration [4]. Typical findings in MRI are irregular “shaggy” enhancing margins with a central necrotic core, surrounded by large T2/fluid-attenuated inversion recovery (FLAIR) hyperintense signal alteration and diffuse non-enhancing tumor infiltration [4]. Given the large temporal intra-axial mass with irregular rim enhancement and the incidence of these tumors in adults between the 6th and 7th decades of life, glioblastoma was considered as the favorite differential diagnosis in this case.
Gliosarcoma
Gliosarcoma (WHO grade 4) is defined as a subtype of IDH wildtype GBM, histologically characterized by a biphasic tissue pattern with glial and mesenchymal differentiation [2, 5]. In MRI, gliosarcomas may either present with a predominant sarcomatous components as a homogeneous Gd-enhancing mass, or with a predominant gliomatous component, resembling GBM [2, 6]. Extracranial involvement in gliosarcomas has been reported in the minority of cases [6]. The superficial location in this case with potential meningeal and ependymal involvement makes gliosarcoma a relevant differential diagnosis in this case.
Metastasis
Metastases represent the most common secondary CNS tumor in adults with roughly 1/3 of all intracranial neoplasms, commonly arising from lung or breast carcinoma or malignant melanoma [7]. They may present as solitary lesion in up to half of cases [7], typically occurring at the gray-white matter junction and may also present with intratumoral hemorrhage [8]. Surrounding edema is often disproportional to the central tumor component [8]. The incidence of cerebral metastases in middle-aged adults and their heterogeneous imaging pattern makes them a relevant differential diagnosis in patients with solitary intra-axial, Gd-enhancing mass lesions. This is also why brain metastasis is certainly a relevant differential diagnosis in this case.
Primary CNS Lymphoma
Primary central nervous system lymphomas (PCNSL) are relatively rare, accounting for only 4% of all intracranial neoplasms, with a peak incidence at about 60 years [2, 9, 10]. Cerebral lymphomas mostly represent mature B‑cell lymphomas [2] and typically present as a hypercellular mass with vivid and homogeneous enhancement after contrast administration, often with restricted diffusion on diffusion weighted imaging (DWI) [11] but may also present with central necrosis, which has been related to Epstein-Barr virus (EBV) positivity [12]. While a solitary manifestation can be observed in the majority of cases, PCNSL may present with multifocal manifestations in about 30–40% of patients [11], often involving the periventricular white matter [2], which is uncommon for brain metastases or GBM. The differentiation between GBM and atypical PCNSL can be improved by using dynamic susceptibility-weighted, contrast-enhanced (DSC) perfusion MRI or even multiparametric approaches [13,14,15]. As this lesion presented as solitary lesion with a large necrotic core within the temporal pole, PCNSL was not considered as the primary differential.
Pleomorphic Xanthoastrocytoma
Pleomorphic xanthoastrocytomas (PXA) WHO grade 2–3 are rare astrocytic tumors accounting for 1% of primary brain tumors, usually seen in the pediatric and young adult population. PXAs typically occur in the supratentorial brain with a predilection for the temporal lobe, commonly related to temporal lobe epilepsy. With a mostly superficial localization, a cyst with Gd-affinitive nodules is often part of the lesion, which in addition often presents with an adjacent lepromeningeal and/or dural Gd-enhancement [2, 16]. Due to long-standing superficial growth, skull remodeling can be found [2, 16]. Regarding the described imaging features of PXA, the diagnosis seems less likely in this older patient with a primary central necrotic lesion, without a circumscribed nodular or cystic tumor component; however, due to the superficial location in the temporal lobe, the diagnosis of PXA needs to be considered.
Histology and Immunohistochemistry
In the hematoxylin and eosin (H&E) stained sections of the formaldehyde-fixed and paraffin-embedded biopsy material, fragments of a highly cellular, diffusely growing tumor with many medium to large sized lymphoid cells were found (Fig. 4). These lymphoid cells exhibited a relatively large, round to oval nucleus with prominent nucleoli, often more than one sticking to the nuclear membrane (Fig. 4). In addition, some tumor cells showed a well-circumscribed cytoplasm of variable size, making them look lymphoblastic-like; however, the tumor cells were mature B cells, labelled positive in the immunohistochemical staining of CD20 and CD79a (Fig. 5). In contrast, T cell markers (CD3) or plasma cell markers (CD38) remained negative within the tumor cells and only stained single scattered cells (Fig. 6). Up to 60% of the tumor cells exhibited expression of MUM1, but expression of CD10 and BCL6 was absent (Fig. 7). BCL2 is expressed by around 80% of the tumor cells; CMYC overexpression is, however, not present. In addition, EBV antigens could not be detected immunohistochemically. Of note, the tumor cells grow in a clearly angiocentric pattern and lie in a dense and diffuse manner next to each other (Fig. 8). The vessels appeared to be split with lymphoid infiltrates. Isolated vessels are clogged. Between these perivascular tumor nodes, necrotic zones appear (Fig. 8). Moreover, larger necrotic areas are found at many sites next to vital tumor tissue. Apoptotic cell bodies can be found, and mitotic activity is brisk; many mitotic figures appear within the tumor. In line with high proliferative activity, up to 80% of the tumor cells are marked in the immunohistochemical staining against Ki-67 (Fig. 9). In summary, the histopathological finding of a highly cellular, highly proliferative, diffusely growing tumor with large B cells (CD20 + CD79+) primarily appearing within the temporal lobe leads to the final diagnosis.
In summary, the histopathological finding of a high cellular, highly proliferative, diffuse growing tumor with large B cells (CD20 + CD79+) primarily appearing within the temporal lobe leads to diagnosing a primary diffuse large B‑cell lymphoma of the CNS.
Diagnosis
Primary Diffuse Large B-cell Lymphoma of the CNS (CNS-DLBCL)
Diffuse large B‑cell lymphoma of the CNS (CNS-DLBCL) is a rare tumor that accounts for 1–3% of primary CNS tumors but is the most common tumor type encountered among primary CNS lymphomas [17, 18]. They typically occur in the cerebral hemispheres (38%) and are less frequent in the thalamus, basal ganglia or cerebellum [19]. For CNS-DLBCL, neither etiological nor genetic predispositions have been described [2]. Macroscopically, CNS-DLBCLs are quite firm and granular, and often exhibit central necrosis [2] as observed in the present case. In general, lymphomas are characterized by nutrient deprivation and hypoxia ultimately leading to tumor necrosis [20]. Interestingly, the presence of necrosis in CT or FDG-PET can serve as a prognostic marker. Patients with tumor necrosis have a significantly worse outcome than those without tumor necrosis [21, 22]. Histologically, tumor cells conform to mature B cells (late germinal center exit), and thus they express typical mature B cell markers such as CD20, CD19, PAX5, or CD79a. In the presented case CD10 expression of the DLBCL was negative arguing against a systemic DLBCL manifestation. CNS-DLBCLs have a significantly worse outcome than systemic DLBCL [23]. The mechanism behind the poor prognosis of CNS-DLBCL is not fully understood. CNS-DLBCLs appear to co-express BCL2, BCL6, and/or MYC at higher frequencies than systemic DLBCL [24]. This co-expression is an established prognostic risk factor [25, 26] and, thus, could point towards potential mechanisms underlying the adverse prognosis of CNS-DLCBL; however, in this case we only found overexpression of BCL2 suggesting a potentially better prognosis. Important differential diagnoses of the CNS-DLBCL include other CNS lymphomas, such as immunodeficiency-associated CNS lymphomas, intravascular large B‑cell lymphoma, or T‑cell and NK/T-cell lymphomas; however, approximately 95% of all primary CNS lymphomas are DLBCL. Only 5% include the mentioned differential diagnosis, and thus, they are exceptionally rare [27].
References
Ostrom QT, Patil N, Cioffi G, Waite K, Kruchko C, Barnholtz-Sloan JS. CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2013–2017. Neuro Oncol. 2020;22(Suppl 2):iv1–iv96.
Louis DN, Perry A, Wesseling P, Brat DJ, Cree IA, Figarella-Branger D, et al. The 2021 WHO classification of tumors of the central nervous system: a summary. Neuro Oncol. 2021;23(8):1231–51.
Marenco-Hillembrand L, Wijesekera O, Suarez-Meade P, Mampre D, Jackson C, Peterson J, et al. Trends in glioblastoma: outcomes over time and type of intervention: a systematic evidence based analysis. J Neurooncol. 2020;147(2):297–307.
Mabray MC, Barajas RF Jr., Cha S. Modern brain tumor imaging. Brain Tumor Res Treat. 2015;3(1):8–23.
Oh JE, Ohta T, Nonoguchi N, Satomi K, Capper D, Pierscianek D, Sure U, Vital A, Paulus W, Mittelbronn M, Antonelli M, Kleihues P, Giangaspero F, Ohgaki H. Genetic alterations in gliosarcoma and giant cell glioblastoma. Brain Pathol. 2016;26:517–22.
Peckham ME, Osborn AG, Palmer CA, Tsai A, Salzman KL. Gliosarcoma: neuroimaging and immunohistochemical findings. J Neuroimaging. 2019;29:126–32.
Achrol AS, Rennert RC, Anders C, Soffietti R, Ahluwalia MS, Nayak L, Peters S, Arvold ND, Harsh GR, Steeg PS, Chang SD. Brain metastases. Nat Rev Dis Primers. 2019;5:5.
Tong E, McCullagh KL, Iv M. Advanced imaging of brain metastases: from augmenting visualization and improving diagnosis to evaluating treatment response. Front Neurol. 2020;11:270.
Smirniotopoulos JG, Jäger HR. Differential diagnosis of intracranial masses. In: Hodler J, Kubik-Huch RA, von Schulthess GK, editors. Diseases of the brain, head and neck, spine 2020–2023: diagnostic imaging. Cham: Springer; 2020. pp. 93–104.
Grommes C, DeAngelis LM. Primary CNS lymphoma. J Clin Oncol. 2017;35:2410–8.
Haldorsen IS, Espeland A, Larsson EM. Central nervous system lymphoma: characteristic findings on traditional and advanced imaging. AJNR Am J Neuroradiol. 2011;32:984–92.
Lee HY, Kim HS, Park JW, Baek HJ, Kim SJ, Choi CG. Atypical imaging features of Epstein-Barr virus-positive primary central nervous system lymphomas in patients without AIDS. AJNR Am J Neuroradiol. 2013;34:1562–7.
Toh CH, Wei KC, Chang CN, Ng SH, Wong HF. Differentiation of primary central nervous system lymphomas and glioblastomas: comparisons of diagnostic performance of dynamic susceptibility contrast-enhanced perfusion MR imaging without and with contrast-leakage correction. AJNR Am J Neuroradiol. 2013;34:1145–9.
Xing Z, You RX, Li J, Liu Y, Cao DR. Differentiation of primary central nervous system lymphomas from high-grade gliomas by rCBV and percentage of signal intensity recovery derived from dynamic susceptibility-weighted contrast-enhanced perfusion MR imaging. Clin Neuroradiol. 2014;24:329–36.
Yu X, Hong W, Ye M, Lai M, Shi C, Li L, Ye K, Xu J, Ai R, Shan C, Cai L, Luo L. Atypical primary central nervous system lymphoma and glioblastoma: multiparametric differentiation based on non-enhancing volume, apparent diffusion coefficient, and arterial spin labeling. Eur Radiol. 2023;33:5357–67.
Molinaro AM, Taylor JW, Wiencke JK, Wrensch MR. Genetic and molecular epidemiology of adult diffuse glioma. Nat Rev Neurol. 2019;15:405–17.
Gerstner ER, Batchelor TT. Primary central nervous system lymphoma. Arch Neurol. 2010;67(3):291–7.
Senocak E, Oguz KK, Ozgen B, Mut M, Ayhan S, Berker M, Ozdemir P, Cila A. Parenchymal lymphoma of the brain on initial MR imaging: a comparative study between primary and secondary brain lymphoma. Eur J Radiol. 2011;79(2):288–94. https://doi.org/10.1016/j.ejrad.2010.01.017.
Küker W, Nägele T, Korfel A, Heckl S, Thiel E, Bamberg M, Weller M, Herrlinger U. Primary central nervous system lymphomas (PCNSL): MRI features at presentation in 100 patients. J Neurooncol. 2005;72(2):169–77. https://doi.org/10.1007/s11060-004-3390-7.
Kluckova K, D’Avola A, Riches JC. Advances in understanding of metabolism of B‑cell lymphoma: implications for therapy. Cancers. 2022;14(22):5552. https://doi.org/10.3390/cancers14225552.
Adams HJA, de Klerk JMH, Fijnheer R, Dubois SV, Nievelstein RAJ, Kwee TC. Prognostic value of tumor necrosis at CT in diffuse large B‑cell lymphoma. Eur J Radiol. 2015;84(3):372–7. https://doi.org/10.1016/j.ejrad.2014.12.009.
Adams HJA, de Klerk JMH, Fijnheer R, Heggelman BGF, Dubois SV, Nievelstein RAJ, Kwee TC. Tumor necrosis at FDG-PET is an independent predictor of outcome in diffuse large B‑cell lymphoma. Eur J Radiol. 2016;85(1):304–9. https://doi.org/10.1016/j.ejrad.2015.09.016.
Korfel A, Schlegel U. Diagnosis and treatment of primary CNS lymphoma. Nat Rev Neurol. 2013;9(6):317–27. https://doi.org/10.1038/nrneurol.2013.83.
Brunn A, Nagel I, Montesinos-Rongen M, Klapper W, Vater I, Paulus W, Hans V, Blümcke I, Weis J, Siebert R, Deckert M. Frequent triple-hit expression of MYC, BCL2, and BCL6 in primary lymphoma of the central nervous system and absence of a favorable MYC(low)BCL2 (low) subgroup may underlie the inferior prognosis as compared to systemic diffuse large B cell lymphomas. Acta Neuropathol. 2013;126(4):603–5. https://doi.org/10.1007/s00401-013-1169-7.
Swerdlow SH, Campo E, Pileri SA, Harris NL, Stein H, Siebert R, Advani R, Ghielmini M, Salles GA, Zelenetz AD, Jaffe ES. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016;127(20):2375–90. https://doi.org/10.1182/blood-2016-01-643569.
Pasqualucci L, Dalla-Favera R. Genetics of diffuse large B‑cell lymphoma. Blood. 2018;131(21):2307–19. https://doi.org/10.1182/blood-2017-11-764332.
Chiavazza C, Pellerino A, Ferrio F, Cistaro A, Soffietti R, Rudà R. Primary CNS lymphomas: challenges in diagnosis and monitoring. Biomed Res Int. 2018;2018:3606970. https://doi.org/10.1155/2018/3606970.
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
M. Frosch, T. Demerath, C. Fung, M. Prinz, H. Urbach, D. Erny and C.A. Taschner declare that they have no competing interests.
Ethical standards
All investigations described in this manuscript were carried out with the approval of the responsible ethics committee and in accordance with national law and the Helsinki Declaration of 1975 (in its current revised form). Informed consent was obtained from the patient in this case if identifiable from pictures or other information within the manuscript.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
The authors M. Frosch and T. Demerath contributed equally to the manuscript.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Frosch, M., Demerath, T., Fung, C. et al. Freiburg Neuropathology Case Conference. Clin Neuroradiol 33, 1159–1164 (2023). https://doi.org/10.1007/s00062-023-01359-y
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00062-023-01359-y