Neurolymphomatosis
Neurolymphomatosis is a rare clinical entity characterized by the infiltration of malignant lymphocytes into the peripheral nervous system. It is most commonly associated with non-Hodgkin's lymphoma, but can also occur in other types of lymphoma. The condition can affect any part of the peripheral nervous system, including the cranial nerves, spinal roots, plexuses, or peripheral nerves.
Etiology[edit | edit source]
The exact cause of neurolymphomatosis is not known. It is believed to occur when malignant lymphocytes infiltrate the peripheral nervous system. This can occur as a result of direct extension from a nearby tumor, or through hematogenous spread. The condition is most commonly associated with non-Hodgkin's lymphoma, but can also occur in other types of lymphoma.
Clinical Presentation[edit | edit source]
Patients with neurolymphomatosis typically present with neurological symptoms, which can vary depending on the part of the peripheral nervous system that is affected. Common symptoms include pain, weakness, sensory loss, and cranial nerve palsies. In some cases, patients may also present with systemic symptoms such as fever, weight loss, and night sweats.
Diagnosis[edit | edit source]
The diagnosis of neurolymphomatosis can be challenging, as the condition can mimic other neurological disorders. A combination of clinical presentation, imaging studies, and nerve biopsy is typically used to establish the diagnosis. Magnetic resonance imaging (MRI) and positron emission tomography (PET) can be useful for identifying areas of nerve involvement. Nerve biopsy can confirm the presence of malignant lymphocytes.
Treatment[edit | edit source]
The treatment of neurolymphomatosis typically involves chemotherapy, with or without radiation therapy. The choice of treatment depends on the type of lymphoma, the extent of nerve involvement, and the patient's overall health. In some cases, surgical resection of the tumor may be considered.
Prognosis[edit | edit source]
The prognosis of neurolymphomatosis is generally poor, with a median survival of less than one year. However, early diagnosis and aggressive treatment can improve survival.
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Contributors: Prab R. Tumpati, MD