An isolated intra-cranial rosai-dorfman disease radiologically mimicking the meningioma
<p>Rosai-Dorfman disease is an uncommon benign non-Langerhans cell histiocytosis proliferative disorder. It commonly involves the lymph nodes and is classically presented with massive cervical lymphadenopathy. It can also involve the extra-nodal sites of the body and is reported in 43% of Rosa...
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International Journal of Radiology and Radiation Oncology - Peertechz Publications,
2022-04-07.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | peertech__10_17352_ijrro_000047 | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Imtiaz Ali |e author |
| 700 | 1 | 0 | |a Ashok Kumar |e author |
| 700 | 1 | 0 | |a Rizwan Ajmal |e author |
| 700 | 1 | 0 | |a Danial Khalid |e author |
| 700 | 1 | 0 | |a Bushra Shamim |e author |
| 700 | 1 | 0 | |a Mahum Zaidi |e author |
| 245 | 0 | 0 | |a An isolated intra-cranial rosai-dorfman disease radiologically mimicking the meningioma |
| 260 | |b International Journal of Radiology and Radiation Oncology - Peertechz Publications, |c 2022-04-07. | ||
| 520 | |a <p>Rosai-Dorfman disease is an uncommon benign non-Langerhans cell histiocytosis proliferative disorder. It commonly involves the lymph nodes and is classically presented with massive cervical lymphadenopathy. It can also involve the extra-nodal sites of the body and is reported in 43% of Rosai-Dorfman disease cases. The central nervous system is rarely involved in Rosai-Dorfman disease from which intra-cranial is more common than spinal lesions. An isolated dural-based intra-cranial Rosai-Dorfman disease is extremely rare. It usually mimics meningioma on radiological imaging. It is very difficult to diagnose the Rosai-Dorfman disease on imaging and intra-operative appearances of the lesion. We present a histopathologically proven case of an isolated Rosai-Dorfman disease involving the central nervous system in 49 years old female patient which was radiologically mimicking the meningioma. </p> | ||
| 540 | |a Copyright © Imtiaz Ali et al. | ||
| 546 | |a en | ||
| 655 | 7 | |a Case Report |2 local | |
| 856 | 4 | 1 | |u https://doi.org/10.17352/ijrro.000047 |z Connect to this object online. |