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Letter
Intrathecal rituximab for IgG4-related hypertrophic pachymeningitis
  1. Emanuel Della-Torre1,2,
  2. Corrado Campochiaro1,2,
  3. Emanuele Bozzalla Cassione1,
  4. Luigi Albano3,
  5. Simonetta Gerevini4,
  6. Stefania Bianchi-Marzoli5,
  7. Enrica Bozzolo2,
  8. Gabriella Passerini6,
  9. Marco Lanzillotta1,
  10. Mariarosa Terreni7,
  11. Marcella Callea7,
  12. Matteo Trimarchi8,
  13. Pietro Mortini3,
  14. Moreno Tresoldi9,
  15. Stefania Acerno3,
  16. Lorenzo Dagna1,2
  1. 1 Università Vita-Salute San Raffaele, Milan, Italy, IRCCS San Raffaele Scientific Institute, Milan, Italy
  2. 2 Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy
  3. 3 Department of Neurosurgery and Gamma Knife Radiosurgery, IRCCS San Raffaele Scientific Institute, Milan, Italy
  4. 4 Neuroradiology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy
  5. 5 Department of Ophthalmology, Fondazione IRCCS Istituto Auxologico Italiano, Neuro-Ophthalmology Service, Milan, Italy
  6. 6 Department of Laboratory Medicine, IRCCS San Raffaele Institute, Milan, Italy
  7. 7 Pathology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy
  8. 8 Department of Otorhinolaryngology, IRCCS San Raffaele Scientific Institute, Milan, Italy
  9. 9 Unit of Medicine and Advanced Care, IRCCS San Raffaele Scientific Institute, Milan, Italy
  1. Correspondence to Emanuel Della-Torre, Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS-San Raffaele Scientific Institute, via Olgettina 60, 20132, Milan, Italy; dellatorre.emanuel{at}hsr.it

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Intrathecal administration of rituximab—an anti-CD20 monoclonal antibody—is emerging as a promising therapeutic strategy for B cell lymphomas of the central nervous system (CNS).1 2 The rationale for administering rituximab directly into the cerebrospinal fluid (CSF) stems from the need to achieve optimal therapeutic concentrations within the intrathecal compartment. Rituximab, in fact, has a high molecular weight and only 0.1%–0.5% of its plasmatic concentrations crosses the ‘blood-brain barrier’ (BBB) after intravenous infusion.1 In addition, despite inducing prolonged depletion of circulating B lymphocytes, systemic rituximab does not affect malignant B cells in CNS lymphomas.2 Hypertrophic pachymeningitis (HP) is the most frequently encountered CNS manifestation of IgG4-related disease (IgG4-RD), a fibroinflammatory condition of unclear aetiology.3 The intrathecal synthesis of IgG4 in patients with IgG4-related hypertrophic pachymeningitis(RHP) and the clinical improvement after rituximab in patients with systemic involvement, support a pathogenic role of B lymphocytes.4–6 Among IgG4-RD manifestations, however, IgG4-RHP stands out for a certain resistance to intravenous rituximab raising the possibility that systemic administration might not be as effective on putative pathogenic B cells residing in inflammatory niches within the CNS.4 Here, we report the first case of IgG4-RHP treated with intrathecal rituximab.

A young adult patient was admitted in April 2015 for rapidly progressive frontal headache and complete visual loss on the right eye. Imaging studies of the head and neck revealed diffuse pachymeningitis with bone erosions, thickening of the nasal septum, hard palate tumefaction, and bilateral optic neuritis; neuro-ophthalmological examination reported asymmetrical signs of optic nerve fibre atrophy (right >left) with loss of colour vision and complete depression of the visual field on the right eye (figure 1 and see online supplementary figure e1). Laboratory and CSF analyses at the time of admission are reported in online …

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Footnotes

  • ED-T and CC contributed equally.

  • Contributors ED-T, CC and EBC conceived the study and wrote the article. LA, SG, SB-M, EB, GP, ML, MC, MrT, MaT, MoT, SA contributed to patient clinical care, data collection and interpretation. PM and LD provided significant advice and supervision, drafting a significant portion of the manuscript. All authors approved the final version of the manuscript. ED-T and CC contributed equally as first authors.

  • Funding This work was supported by “Fondazione Italiana per la Ricercasull’Artrite” (FIRA Onlus 2014) and by the “Collegio Ghislieri” (Pavia).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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