nach oben

Clinical Neuroradiology

Erschienen in:

01.03.2013 | Clinical Case

Freiburg Neuropathology Case Conference: A Partially Calcified, Dura-based Tumour of the Frontal Lobe

verfasst von: C. A. Taschner, O. Staszewski, R. Jabbarli, A. Keuler, M. Prinz

Erschienen in: Clinical Neuroradiology | Ausgabe 1/2013

Einloggen, um Zugang zu erhalten

Excerpt

A 50-year-old female patient was admitted to a county hospital after an accident due to a first-time generalised seizure with anterograde amnesia. Computed tomography (CT) and magnetic resonance imaging (MRI) revealed a parasagittal convexity lesion in the right frontal lobe. The patient received antiepileptic medication and was referred to our university hospital for surgery. A right frontal craniotomy for microsurgical tumour resection was performed. The oval-shaped tumour with the diameter of about 25 mm was adherent to convexity dura, possessed a solid consistency with own capsule and well-defined arachnoid border to surrounding frontal cortex. Macroscopically the tumours seemed compatible with the diagnosis of a convexity meningioma. After excision of affected convexity dura, a complete microsurgical resection of lesion could be achieved. Postoperatively, the patient had no neurological deficit and no seizures under continued antiepileptic medication. After proper recovery she was discharged. A routine ambulatory check-up 2 months after surgery revealed no new clinical complaints; in the absence of seizures the antiepileptic medication was reduced. …

Nayak L, Abrey LE, Iwamoto FM. Intracranial dural metastases. Cancer. 2009;115:1947–53.PubMedCrossRef

Campbell BA, Jhamb A, Maguire JA, Toyota B, Ma R. Meningiomas in 2009: controversies and future challenges. Am J Clin Oncol. 2009;32:73–85.PubMedCrossRef

Shah R, Roberson GH, Curé JK. Correlation of MR imaging findings and clinical manifestations in neurosarcoidosis. AJNR Am J Neuroradiol. 2009;30:953–61.PubMedCrossRef

Yamaki T, Ikeda T, Sakamoto Y, Ohtaki M, Hashi K. Lymphoplasmacyte-rich meningioma with clinical resemblance to inflammatory pseudotumor. Report of two cases. J Neurosurg. 1997;86(5):898–904.PubMedCrossRef

Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Editors. WHO classification of tumours of the central nervous system. Lyon: IARC; 2007.

Glidden D, Grau J, Bagg A. Reactive versus neoplastic lymphoid follicles: proliferation and death versus quiescence and staying alive. Br J Haematol. 2004;126(6):757.PubMedCrossRef

Magliozzi R, Howell O, Vora A, Serafini B, Nicholas R, Puopolo M, et al. Meningeal B-cell follicles in secondary progressive multiple sclerosis associate with early onset of disease and severe cortical pathology. Brain. 2006;130(4):1089–104.CrossRef

Kuo T, Chen T, Lee L, Lu P. IgG4-positive plasma cells in cutaneous rosai-dorfman disease: an additional immunohistochemical feature and possible relationship to IgG4-related sclerosing disease. J Cutan Pathol. 2009;36(10):1069–73.PubMedCrossRef

Roberts S, Attanoos R. IgG4+ Rosai-Dorfman disease of the lung. Histopathology. 2010;56(5):662–4.PubMedCrossRef

10.

Chen TD, Lee LY. Rosai-dorfman disease presenting in the parotid gland with features of IgG4-related sclerosing disease. Arch Otolaryngol Head Neck Surg. 2011;137(7):705–8.PubMedCrossRef

11.

Cha Y, Yang W, Park S, Koo J. Rosai-dorfman disease in the breast with increased IgG4 expressing plasma cells: a case report. Korean J Pathol. 2012;46(5):489–93.PubMedCrossRef

12.

Richter J, Strange R, Fisher S, Miller D, Delvecchio D. Extranodal rosai-dorfman disease presenting as a cardiac mass in an adult: report of a unique case and lack of relationship to IgG4-related sclerosing lesions. Hum Pathol. 2010;41(2):297–301.PubMedCrossRef

13.

Hamano H, Kawa S, Horiuchi A, Unno H, Furuya N, Akamatsu T, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med. 2001;344(10):732–8.PubMedCrossRef

14.

Kamisawa T, Funata N, Hayashi Y, Tsuruta K, Okamoto A, Amemiya K, et al. Close relationship between autoimmune pancreatitis and multifocal fibrosclerosis. Gut. 2003;52(5):683–7.PubMedCrossRef

15.

Shrestha B, Sekiguchi H, Colby T, Graziano P, Aubry MC, Smyrk TC, et al. Distinctive pulmonary histopathology with increased IgG4-positive plasma cells in patients with autoimmune pancreatitis: report of 6 and 12 cases with similar histopathology. Am J Surg Pathol. 2009;33(10):1450–62.PubMedCrossRef

16.

Zen Y, Harada K, Sasaki M, Sato Y, Tsuneyama K, Haratake J, et al. IgG4-related sclerosing cholangitis with and without hepatic inflammatory pseudotumor, and sclerosing pancreatitis-associated sclerosing cholangitis: do they belong to a spectrum of sclerosing pancreatitis? Am J Surg Pathol. 2004;28(9):1193–203.PubMedCrossRef

17.

Yoneda K, Murata K, Katayama K, Ishikawa E, Fuke H, Yamamoto N, et al. Tubulointerstitial nephritis associated with IgG4-related autoimmune disease. Am J Kidney Dis. 2007;50(3):455–62.PubMedCrossRef

18.

Chan S, Cheuk W, Chan K, Chan J. IgG4-related sclerosing pachymeningitis: a previously unrecognized form of central nervous system involvement in IgG4-related sclerosing disease. Am J Surg Pathol. 2009;33(8):1249–52.PubMedCrossRef

19.

Choi S, Lee S, Khang S, Jeon S. IgG4-related sclerosing pachymeningitis causing spinal cord compression. Neurology. 2010;75(15):1388–90.PubMedCrossRef

20.

Kosakai A, Ito D, Yamada S, Ideta S, Ota Y, Suzuki N. A case of definite IgG4-related pachymeningitis. Neurology. 2010;75(15):1390–2.PubMedCrossRef

21.

Lindstrom KM, Cousar JB, Lopes M. IgG4-related meningeal disease: clinico-pathological features and proposal for diagnostic criteria. Acta Neuropathol. 2010;120(6):765–76.PubMedCrossRef

22.

Moss HE, Mejico L, de la Roza G, Coyne TM, Galetta SL, Liu G. IgG4-related inflammatory pseudotumor of the central nervous system responsive to mycophenolate mofetil. J Neurol Sci. 2012;318(1–2):31–5.PubMedCrossRef

23.

Katsura M, Morita A, Horiuchi H, Ohtomo K, Machida T. IgG4-related inflammatory pseudotumor of the trigeminal nerve: another component of IgG4-related sclerosing disease? AJNR Am J Neuroradiol. 2011;32(8):E150–2.PubMedCrossRef

Titel: Freiburg Neuropathology Case Conference: A Partially Calcified, Dura-based Tumour of the Frontal Lobe
verfasst von: C. A. Taschner
O. Staszewski
R. Jabbarli
A. Keuler
M. Prinz
Publikationsdatum: 01.03.2013
Verlag: Springer-Verlag
Erschienen in: Clinical Neuroradiology / Ausgabe 1/2013
Print ISSN: 1869-1439
Elektronische ISSN: 1869-1447
DOI: https://doi.org/10.1007/s00062-013-0199-9

Update Radiologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

Newsletter bestellen

Die Highlights vom Kongress des American College of Cardiology 2024

Springer Medizin

Freiburg Neuropathology Case Conference: A Partially Calcified, Dura-based Tumour of the Frontal Lobe

Excerpt

Neu im Fachgebiet Radiologie

Darf man die Behandlung eines Neonazis ablehnen?

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

Endlich: Zi zeigt, mit welchen PVS Praxen zufrieden sind

Akuter Schwindel: Wann lohnt sich eine MRT?

Update Radiologie

Die Highlights vom Kongress des American College of Cardiology 2024

Springer Medizin

Excerpt

Bitte loggen Sie sich ein, um Zugang zu diesem Inhalt zu erhalten

Weitere Artikel der Ausgabe 1/2013

Solitary Spinal Extradural Plasmacytoma: A Case Report and Literature Review

Retraction Note to: Familial Aplasia of the Olfactory Bulb

Cervical Artery Dissection in a Young Patient with Rubinstein-Taybi Syndrome

Societies Communications

Bilateral Persistent Primitive Trigeminal Arteries Associated with Trigeminal Neuralgia

IMS-3, SYNTHESIS, and MR RESCUE: No Disaster, but Down to Earth

Neu im Fachgebiet Radiologie

Darf man die Behandlung eines Neonazis ablehnen?

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

Endlich: Zi zeigt, mit welchen PVS Praxen zufrieden sind

Akuter Schwindel: Wann lohnt sich eine MRT?

Update Radiologie