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Jia et al.                                                                                                                                                                       GBS after cerebral hemorrhage or trauma

           some support and hold light objects.               are elevated in patients with post  traumatic head
                                                              injury.  Some studies have shown that nearly 80% of
                                                                   [3]
           DISCUSSION                                         AMAN patients are anti-ganglioside antibody positive,
                                                              especially  within  the  first  week  of  onset.   The  best
                                                                                                   [4]
           We reported two patients with severe GBS following   treatment for GBS is IVIg or plasma exchange, both
           cerebral hemorrhage or head trauma. In the two     of  which aim to remove antibodies. However,  serum
           cases above, typical clinical manifestations were the   anti-ganglioside  antibodies  were negative in case 1.
           sudden  occurrence  of  flaccid  tetraplegia,  areflexia,   We postulate 2 possible explanations: one is that the
           hypomyotonia, and respiratory failure, without any   antibody level had decreased sharply after 2 courses
           sensory  dysfunction.  NCS  of  both  patients  showed   of IVIg when it was obtained 17 days after onset; the
           decreased  CMAP  and  prolonged  distal  F  wave   other is the patient suffered from anti-ganglioside
           latencies,  indicating  motor  axon  injury,  which  are   antibody  negative  GBS.  The 2 patients  reported
           common electrophysiological features of  AMAN.     showed significant recovery due to prompt diagnosis
           In  addition,  the  result  of  the  CSF  tests  indicated   and treatment.
           albumino-cytologic dissociation, and IVIg proved to be
           efficient in both patients.                        In clinical practice, if a sudden bilateral limb weakness
                                                              occurs after traumatic injury or hemorrhage,  which
           The most common subtypes of GBS are acute          cannot be explained by findings of imaging and routine
           inflammatory  demyelinating  polyradiculoneuropathy   laboratory examinations, GBS should be considered.
                                                                                                            [14]
           (AIDP) and AMAN. In contrast to North America and   Early examination of the nervous system, EMG, CSF
           Europe, where more than 90% of the patients are    test,  and  search  for  anti-ganglioside  antibodies can
           classified as AIDP, approximately 65% of patients in   support the diagnosis of peripheral nerve demyelinating
           China suffer from AMAN, a subtype of GBS with only   disease.  For  patients  diagnosed  with  GBS,  gamma
           motor  fiber  damage.  Analogous to our cases, the   globulin should be given as soon as possible, if there are
                              [8]
           features of nerve conduction studies demonstrated   no contraindications, otherwise plasma exchange can
           decreased  motor  amplitudes  with  an  absence  of  F   be used.  Despite the rare reports of GBS following
                                                                      [15]
           waves.                                             head  trauma  or  brain  hemorrhage,  we  find  that  it  is
                                                              not as rare as we thought in clinical practice. GBS is
           The exact pathogenesis of GBS following brain trauma   not a common disease  and it is easy to be ignored
           and hemorrhage is not completely clear. Tan  et al.    or misdiagnosed, especially  following  other severe
                                                          [6]
           performed sural nerve biopsy and found phagocytosis   situations like trauma and brain hemorrhage.  Thus,
           of myelin sheath debris in the endoneurium.  Tan   it  is  of  great  significance  to  enhance  the  awareness
           suggested that head trauma and surgery had elevated   of early diagnosis and early treatment of this special
           serum  and  CSF  myelin  basic  protein  levels,  which   pathogenic GBS, which will increase the survival rate
           led to immune system activation to produce anti-   and improve the quality of patients’ life.
           myelin antibodies that cause demyelination. Moreover,
           relevant literature indicates that  blood-brain  barrier   Authors’ contributions
           (BBB) damage plays an important role in post-      Collection of study cases and problem analysis: H. Jia
           traumatic GBS pathogenesis. [9,10]  Disintegration of the   Writing of the paper and critical revision of the article:
           BBB during  neurotrauma  leads  to the accumulation   H. Jia, B. Li
           of localized T lymphocytes and macrophages, which   Revised article: H. Jia, Y. Tian, Y.M. Wu
           may induce the transformation of microglial  cells in
           the nervous system into antigen presenting cells. [3,11,12]    Financial support and sponsorship
           Activated microglia can present post traumatic neuronal   None.
           debris to the immune system and stimulate B cells to
           produce antibodies against the myelin sheath, causing   Conflicts of interest
           demyelination,  especially  in the peripheral  nervous   There are no conflicts of interest.
           system.   The explanation  of GBS following  head
                  [13]
           trauma or hemorrhage may be that some substances   Patient consent
           originating in the central nervous system, usually being   Consent was approved by patients in both cases.
           weakly  immunogenic,  are transported  through  the
           disrupted BBB to the peripheral nervous system where   Ethics approval
           they cause demyelination or axonal damage.         Data collection  in our study involving  the patient is
                                                              consistent with the ethical standards of the institution’s
           It has been reported that anti-ganglioside  antibodies   ethics committee.
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