Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Ataxia

Cerebellar ataxia refers to ataxia due to dysfunction of the cerebellum. This causes a variety of elementary neurological deficits including asynergy (lack of coordination between muscles, limbs and joints), dysmetria (lack of ability to judge distances that can lead to under- oder overshoot in grasping movements), and dysdiadochokinesia (inability to perform rapid movements requiring antagonizing muscle groups to be switched on and off repeatedly).


合計: 7

                       


（表示件数）
PMID (PMCID)
27920713
(5121570)
 OTHER
Late-Onset Langerhans Cell Histiocytosis with Cerebellar Ataxia as an Initial Symptom.
Pyun JM, Park H, Moon KC, Jeon B.
Case Rep Neurol. 2016;8(3):218-223.
Late-Onset Langerhans Cell Histiocytosis with Cerebellar Ataxia as an Initial Symptom.
27920713
(5121570)
 OTHER
Late-Onset Langerhans Cell Histiocytosis with Cerebellar Ataxia as an Initial Symptom.
Pyun JM, Park H, Moon KC, Jeon B.
Case Rep Neurol. 2016;8(3):218-223.
The mass, lytic lesion of the skull, white matter lesion, diabetes insipidus, and cerebellar ataxia all suggested a final diagnosis of Langerhans cell histiocytosis (LCH), which was confirmed histopathologically.
15543008
 MALE Infant
Cerebellar ataxia in pediatric patients with Langerhans cell histiocytosis.
Imashuku S, Ishida S, Koike K, Ichikawa M, Minato T, Suzuki Y, Kobayashi R, Morimoto A.
J Pediatr Hematol Oncol. 2004;26(11):735-9.
Cerebellar ataxia in pediatric patients with Langerhans cell histiocytosis.
11453455
 MIXED_SAMPLE Infant
Delayed diagnosis of pediatric Langerhans' cell histiocytosis: case report and retrospective review of pediatric cases seen at Mayo Clinic.
Jarquin-Valdivia AA, Buchhalter J.
J Child Neurol. 2001;16(7):535-8.
Our findings indicate that neurologic manifestations of Langerhans' cell histiocytosis are rare, and the combination of diabetes insipidus, ataxia, skin rash, or osseous pain should alert the clinician to the possibility of Langerhans' cell histiocytosis and avoid delayed diagnosis.
11453455
 MIXED_SAMPLE Infant
Delayed diagnosis of pediatric Langerhans' cell histiocytosis: case report and retrospective review of pediatric cases seen at Mayo Clinic.
Jarquin-Valdivia AA, Buchhalter J.
J Child Neurol. 2001;16(7):535-8.
Our findings indicate that neurologic manifestations of Langerhans' cell histiocytosis are rare, and the combination of diabetes insipidus, ataxia, skin rash, or osseous pain should alert the clinician to the possibility of Langerhans' cell histiocytosis and avoid delayed diagnosis.
10051019
 MALE Child
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndrome.
Di Rocco M, Arslanian A, Romanengo M, Dagna-Bricarelli F, Borrone C.
J Med Genet. 1999;36(2):159-60.
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndrome.
302803
 FEMALE Middle Aged
Histiocytosis X in adult with skin and uncommon central nervous system involvement.
Amirdjazil Z, Esca SA, Konrad K.
Dermatologica. 1977;155(5):283-91.
Report of a case of histiocytosis X with adult onset, widespread skin lesions and rare central nervous system involvement resulting in dizziness and ataxia.