Case reports and Correspondence

Rajeswari, Binitha; Krishnan, Syam; Sarada, C; Kusumakumary, P; Mehta, Kumud; More, Vaishali; Chitale, Arun R.; Khubchandani, Shaila; Kaur, Anupam; Khetarpal, Shailesh; Kumar, Arvind; Asaf, Belal Bin; Chugh, Krishan; Talwar, Neetu; Sanklecha, Mukesh; Sundaresan, Suba; Reddy, K. R. Bharath Kumar; Biswas, Asthik; Sahu, Jitender Kumar; Singh, Varinder; Sharath, B. N.; Kumar, Chandra Mohan; Patwari, A. K.; Kaur, Baljinder; Gupta, Aashray K.

doi:10.1007/s13312-013-0201-2

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Guillain-barre Syndrome As a Paraneoplastic Phenomenon In A ...1

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Cited by 8 publications

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“…The cases so far reported, three were in the B cell type ALL and had AMAN variant. [ 6 7 8 ] Except two cases, all were described during induction therapy and onset was in 3–5 weeks of therapy. Almost all cases had albuminocytological dissociation in CSF.…”

Section: Discussionmentioning

confidence: 99%

Guillain-Barre syndrome in acute lymphoblastic leukemia: Causal or coincidental

et al. 2015

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Section: Discussionmentioning

confidence: 99%

Guillain-Barre syndrome in acute lymphoblastic leukemia: Causal or coincidental

et al. 2015

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“…To the Editor: Acute lymphoblastic leukemia (ALL) is the most common malignancy seen in children. Paraneoplastic neuropathies are rarely encountered in children with ALL, 1 but have been described more frequently in adults with other hematologic malignancies. [2][3][4] Here, we describe a patient with B-cell ALL and t(8;22) who developed Guillain-Barre syndrome (GBS) as a paraneoplastic phenomenon.…”

Section: Guillain-barre Syndrome As a Paraneoplastic Phenomenon In A ...mentioning

confidence: 99%

Guillain–Barre syndrome as a paraneoplastic phenomenon in a child with MYC rearranged B‐cell acute lymphoblastic leukemia

Cooksey,

Kubaney,

Loudamy

et al. 2024

Pediatric Blood & Cancer

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LETTER TO THE EDITORNerve dysfunction is commonly seen in patients with ALL, and may be related to central nervous symptom involvement by leukemia or side effects of chemotherapy drugs, particularly vincristine. 8 GBS is rarely recognized as a paraneoplastic phenomenon in cancer, and its presenting symptoms may be difficult to discern from more common causes of neurologic impairment. Its prompt recognition and GBS-specific therapy alongside cancer-directed therapy may allow for significant neurologic recovery.Autoantibody production and autoimmune effects have often been described in patients with Burkitt lymphoma, 9-11 but this phenomenon is recognized less often in B-cell ALL. B-cell ALL characterized by t(8;22) is a rarely encountered subtype that may be associated with a lymphomatous clinical presentation and production of autoantibodies responsible for paraneoplastic phenomena.

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