Program Operations Manual System (POMS)
TN 57 (08-23)
DI 23022.633 Paraneoplastic Cerebellar Degeneration
COMPASSIONATE ALLOWANCES INFORMATION
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PARANEOPLASTIC CEREBELLAR DEGENERATION
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ALTERNATE NAMES
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Paraneoplastic Cerebellar Ataxia; PCD; Rapidly Progressive Cerebellar Syndrome; Subacute
Cerebellar Degeneration
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DESCRIPTION
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Paraneoplastic Cerebellar Degeneration (PCD) is paraneoplastic syndrome caused by “killer T-cells,” or cytotoxic CD8+ T lymphocytes
attacking normal cells in the cerebellum. Paraneoplastic syndromes are conditions
believed to be the result of abnormal responses to undetected underlying malignant
tumors.
PCD is a rare, non-metastatic complication that occurs in less than 1% of cancer patients
(children and adults). Individuals with ovarian cancer, uterine cancer, breast cancer,
small-cell lung cancer, and Hodgkin lymphoma are most often affected by PCD.
The symptoms of PCD can be rapidly progressive and very debilitating and they typically
precede the diagnosis of the underlying malignancy. Prompt recognition and treatment
of this disease are crucial to the prevention of significant disability.
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DIAGNOSTIC TESTING, PHYSICAL FINDINGS, AND ICD-9-CM/ICD-10-CM
CODING
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Diagnostic testing: The diagnosis of PCD is typically made by ruling out more common conditions that
affect the cerebellum and other neurological disorders.
Testing used to diagnosis PCD may include:
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Computed tomography scans (CT);
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Various blood test panels;
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Magnetic resonance imaging (MRI)(MRI of the brain in PCD is usually normal but can
show cerebellar atrophy as the disease progresses);
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Fluorodeoxyglucose-positron emission tomography scan; and
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Positron emission tomography-computed tomography (PET/CT).
Physical findings: Physical findings of individuals with PCD may include:
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Ataxia (loss of coordination);
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Dysarthria (slurred speech);
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Dysphagia (difficulty swallowing);
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Nystagmus (dancing eyes); and
ICD-9: 331.89
ICD-10: G31.9, G32.81
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PROGRESSION
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Symptoms of PCD usually precede the diagnosis of the underlying cancer diagnosis.
They often present very mildly and progress rapidly before ultimately reaching a severely
disabled state that is followed by a variable plateau period that can last for months
to years.
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TREATMENT
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Treatment of PCD varies depending on the source and severity of the underlying tumor.
Common treatment for the condition may include tumor removal, high dose gammaglobulin
therapy, or immunotherapy.
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SUGGESTEDPROGRAMMATIC ASSESSMENT*
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Suggested MER for Evaluation:
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Clinical history and physical examination that describes the diagnostic features of
the impairment including a description of gait; and
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Imaging Reports Results of imaging (CT scan, MRI, PET).
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Suggested Listings for Evaluation:
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DETERMINATION
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LISTING
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REMARKS
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Meets
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11.17
111.17
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PCD in adults must meet the conditions of 11.17 A or 11.17 B.
PCD in children must meet the conditions of 111.17.
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Equals
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* Adjudicators may, at their discretion, use the Medical Evidence of Record or the
listings suggested to evaluate the claim. However, the decision to allow or deny the
claim rests with the adjudicator.
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