A case of periodic sweating associated with a subarachnoid cyst and multifocal dystonia

1993 ◽  
Vol 3 (5) ◽  
pp. 299-301 ◽  
Author(s):  
Ana Lucia Z. Rosso ◽  
James P. Mattos ◽  
Sérgio A. P. Novis
Keyword(s):  
Subarachnoid Cyst

Posttraumatic spinal subarachnoid cyst

1996 ◽  
Vol 6 (4) ◽  
Author(s):  
C.M. Coffin ◽  
A. Weill ◽  
Y. Miaux ◽  
A. Srour ◽  
C. Cognard ◽  
...  
Keyword(s):  
Subarachnoid Cyst

Leptomeningeal cysts in congenital ectopia lentis

1973 ◽  
Vol 38 (5) ◽  
pp. 650-654 ◽  
Author(s):  
Bryce Weir
Keyword(s):  
Connective Tissue ◽  
Marfan Syndrome ◽  
Genetic Disorder ◽  
Ectopia Lentis ◽  
Content Type ◽  
Extradural Cyst ◽  
Common Pathogenesis ◽  
Intrathoracic Meningocele ◽  
Subarachnoid Cyst ◽  
Fine Print

✓ A case of ectopia lentis (Marfan syndrome) with a cerebral subarachnoid cyst, a spinal extradural cyst connected to a lateral intrathoracic meningocele, and perineural cysts is presented. The association of these leptomeningeal cysts in this genetic disorder of connective tissue suggests a common pathogenesis.

SPINAL SUBARACHNOID CYST IN A CAT

1999 ◽  
Vol 40 (2) ◽  
pp. 116-119 ◽  
Author(s):  
Massimo Vignoli ◽  
Federica Rossi ◽  
Giuseppe Sarli
Keyword(s):  
Subarachnoid Cyst

scholarly journals Malignant infantile osteopetrosis with rickets presenting with bicytopenia in septic shock: case report

2021 ◽  
Vol 8 (7) ◽  
pp. 1268
Author(s):  
Varun Govindarajan ◽  
Thanzir Mohammed ◽  
Meghana Jagadish ◽  
Mallesh Kariyappa
Keyword(s):  
Septic Shock ◽  
Autosomal Recessive ◽  
Hematopoietic Stem Cell Transplant ◽  
Married Couple ◽  
Delayed Diagnosis ◽  
Failure To Thrive ◽  
Autosomal Recessive Disorder ◽  
Cell Transplant ◽  
Hematopoietic Stem ◽  
Subarachnoid Cyst

Malignant infantile osteopetrosis is a rare, fatal autosomal recessive disorder due to abnormal osteoclast activity. We report a 1-year-old infant, born to consanguineously married couple, who presented to our ER with acute respiratory distress and bicytopenia. He had tender hepatomegaly, splenomegaly, failure to thrive and features of rickets. He was evaluated previously for possible hydrocephalus secondary to his abnormal shape of head with proptosis, MRI revealed a subarachnoid cyst, but possibility of osteopetrosis was missed. Skeletal radiographs done later detected dense, sclerotic bone with sandwich vertebra, provided a delayed diagnosis of MIOP. Rickets, a paradoxical association, was also seen in our case, with low serum calcium and vitamin D3 levels. He succumbed due to severe bronchopneumonia with septic shock. Early diagnosis and timely hematopoietic stem cell transplant are the only curative approach for MIOP, which is otherwise fatal.

Multiple Thoracic Intradural Subarachnoid Cyst: A Case Report

2008 ◽  
Vol 57 (1) ◽  
pp. 106-109
Author(s):  
Masahiro Kubo ◽  
Takayoshi Ueta ◽  
Keiichiro Shiba ◽  
Eiji Mori ◽  
Kozo Kaji ◽  
...  
Keyword(s):  
Case Report ◽  
Subarachnoid Cyst

Subarachnoid cyst in a cat

1997 ◽  
Vol 33 (2) ◽  
pp. 123-125 ◽  
Author(s):  
MH Shamir ◽  
R Shahar ◽  
I Aizenberg
Keyword(s):  
Contrast Material ◽  
Cord Compression ◽  
Neurological Deficits ◽  
Thoracic Vertebrae ◽  
Neurological Signs ◽  
The Third ◽  
Limb Ataxia ◽  
Intradural Extramedullary ◽  
Subarachnoid Cyst

A five-year-old domestic longhair was presented with hind-limb ataxia and some degree of incontinence of two weeks' duration. An enlarged spinal canal from the twelfth thoracic (T12) vertebra to the third lumbar (L3) vertebra was identified on survey radiographs. An intradural-extramedullary cavity at the twelfth (T12) and thirteenth (T13) thoracic vertebrae, filled with contrast material, was demonstrated on myelography. A left-sided hemilaminectomy was performed over this region, and a subarachnoid cavitation or cyst was found to be the cause of the severe spinal-cord compression. The cyst was drained. The cat showed improvement in the neurological signs during the first three weeks postoperatively. Six months later, no neurological deficits were identified on follow-up examination.

Subarachnoid Cyst Simulating an Intracanalicular Acoustic Neuroma

1981 ◽  
Vol 89 (6) ◽  
pp. 1019-1020 ◽  
Author(s):  
Steven M. Parnes ◽  
Louis R. Nelson
Keyword(s):  
Case Report ◽  
Acoustic Neuroma ◽  
Cerebellopontine Angle ◽  
Review Of The Literature ◽  
The Third ◽  
Acoustic Neuromas ◽  
Subarachnoid Cyst

Acoustic neuromas are the most common lesions found in the cerebellopontine angle. A subarachnoid cyst rarely involves this area. A review of the literature indicates that this is only the third case report in which the subarachnoid cyst manifested itself clinically and radiographically as an intracanalicular acoustic neuroma.

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