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MEDICAL GRANDROUNDS. Marion Priscilla B. Aurellado, M.D. May 22, 2008. Objectives. To present a case of cerebral toxoplasmosis To discuss an approach to right upper extremity weakness in a young, previously healthy patient with mass lesions in the brain on imaging
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MEDICAL GRANDROUNDS Marion Priscilla B. Aurellado, M.D. May 22, 2008
Objectives • To present a case of cerebral toxoplasmosis • To discuss an approach to right upper extremity weakness in a young, previously healthy patient with mass lesions in the brain on imaging • To present some epidemiologic data on the burden of HIV/AIDS in the Philippines
Identifying Data • J.E. • 27 year old male • Single • Filipino • Roman Catholic • From Pangasinan
Chief Complaint • Near syncopal attack
3 months Intermittent dizziness Light headedness No meds/consult History of Present Illness
2 weeks RUE weakness Weak hand grip Orthopedic consult done Unrecalled meds given Advised observation Progression of right weakness Follow-up consult done EMG-NCV advised, but not done History of Present Illness
2 days Admission generalized body weakness Near syncopal attack Clinic consult done Hypotensive at 80/60 Advised admission History of Present Illness
(+) weight loss ~ 30 lbs in 4 months (+) undocumented intermittent fever & chills since 4 months (+) anorexia (+) hair loss (-) headache (-) loss of consciousness (-) cough or colds (-) chest pain (-) dyspnea (-) palpitations (-) abdominal pain (-) nausea or vomiting (-) LBM/constipation (-) melena (-) hematochezia (-) dysuria (-) hematuria Review of Systems
Past Medical History • No asthma • No DM • No history of hepatitis • No previous hospitalizations • No history of blood transfusions • No known food or drug allergies
Family History • (+) DM
Social History • Non-smoker • Occasional alcoholic beverage drinker • No illicit drug use
Physical Examination • General Survey: Conscious, coherent, not in respiratory distress • Vital Signs: BP lying: 100/60 BP sitting: 100/60 BP standing: 80/50 CR 88 RR 18 afebrile • HEENT: Pink palpebral conjunctivae, anicteric sclerae, (-) tonsillopharyngeal congestion, (-) cervical lymphadenopathies
Physical Examination • Chest & Lungs: Symmetric chest expansion, clear breath sounds • CVS: Adynamic precordium, normal rate, regular rhythm, no murmurs • Abdomen: Flat abdomen, normoactive bowel sounds, no tenderness, no organomegaly
Physical Examination • Extremities: Full and equal pulses, no edema, (+) purplish skin rash all over, (+) atrophy of dorsal interossei muscles of right hand (claw hand appearance), (+) subcutaneous nodules in all extremities
Neurologic Examination • Mental Status Exam: awake, oriented to 3 spheres no memory lapses, good attention intact repetition, recall 3/3 no aphasia, no R-L disorientation
Neurologic Examination • Cranial Nerves: CN I - intact CN II – pupils 3-4 mm EBRTL, visual fields intact CN III, IV, VI – primary gaze midline, full EOMs CN V – intact V1-V3 CN VII – no facial asymmetry CN VIII - intact CN IX, X – intact gag CN XI – good SCM tone CN XII – tongue midline
Neurologic Examination • Sensory: Intact to all modalities • Motor: 5/5 on both lower extremities and LUE RUE: 5-/5 shoulder abduction 4/5 shoulder adduction 4/5 Shoulder extension 5-/5 shoulder flexion 5-/5 elbow flexion 4/5 elbow extension
Neurologic Examination • Cerebellum: No dysdiadochoinesia, no dysmetria, able to walk in tandem, walk on heels and toes • Deep Tendon Reflexes: +2 left; +3 right upper extremity, +2 right lower extremity • Pathologic Reflexes: no Babinski • Meninges: no nuchal rigidity
Salient Features • 27 year old male • Previously healthy • Right upper extremity weakness, dizziness • Significant weight loss & anorexia • Intermittent fever • Generalized skin rash • Atrophy of dorsal interossei muscles of right hand (claw hand appearance) • Subcutaneous nodules in all extremities
Where is the Lesion? • Focal peripheral nerve involvement
What is the Nature of the Lesion? • Metabolic • Inflammatory • Trauma Thomas PK, Ochoa J. Symptomatology and differential diagnosis of peripheral neuropathy. In: Dyck PJ, Thomas PK, eds. Peripheral neuropathy. Philadelphia: Saunders, 1993:749-74.
Admitting Impression • Connective Tissue Disease
Course in the Wards • 12 L ECG • Stat 5 • IV Fluids started • ESR and ANA • EMG-NCV
1st Hospital Day • BP stable 100-110/60-70 • No dizziness • (+) R arm weakness • ESR 120 • Impression: Connective tissue disease
2nd Hospital Day • Prednisone started • EMG NCV R arm - NORMAL • ANA negative • Impression: Connective tissue disease ruled out
2nd Hospital Day • Repeat CBC • Anemia & eosinophilia • Fecalysis • Dermatology referral: Skin biopsy • Impression: Parasitic infection • MRI & MRA with Gadolinium
Salient Features • Subcutaneous nodules in all extremities • Anemia, eosinophilia • Multiple ring enhancing lesions on cranial MRI • Impression: T/C Neurocysticercosis R/O CNS Malignancy
Multiple Ring Enhancing Lesions on MRI Neoplastic Infectious Primary Metastatic
Multiple Ring Enhancing Lesions on MRI Neoplastic Infectious Bacterial Abscess Tuberculoma Cryptococcus Toxoplasmosis Neurocysticercosis
Primary CNS Lymphoma • Present with one of 3 syndromes • Subacute progression of focal neurologic deficit • Seizure • Nonfocal neurologic deficit: Headache • Fever, malaise, weight loss, anorexia suggest metastatic more than primary • Uniformly enhancing mass lesion in immunocompetent • Ring enhancing in the immunocompromised
Metastatic Brain Tumors • Most commonly originates from: • Lung CA • Breast CA • GI malignancy • Melanoma
Bacterial Brain Abscess • Cause: Streptococcus (40%), Anaerobes, Staphylococcus (10%) • Associated with otitis, mastoiditis, dental infections or head trauma • Headache is the most common symptom in >75% of cases • Classic triad of headache, fever, and focal neurologic deficit • Multiple hematogenous poorly encapsulated
Tuberculoma • Uncommon manifestation of CNS tuberculosis • Cause: Mycobacterium tuberculosis • Transmission: Hematogenous spread from a primary pulmonary or postprimary pulmonary disease • Seizures or focal neurologic deficits • Diagnosis: AFB on CSF
Neurocysticercosis • Cause: Taenia solium • Transmission: Ingestion of undercooked pork • Cysticerci found anywhere in the body but are commonly in: • Brain • CSF • Skeletal muscle • Subcutaneous tissue • Eye
Neurocysticercosis • Often presents with seizures and signs of increased intracranial pressure • Diagnosis: • Fecalysis • Neuroimaging • Evidence of cysticercosis outside the CNS
Cryptococcosis • Cause: Cryptococcus neoformans • Transmission: inhalation of yeast from the environment (bird droppings) • Risk factor: CD4 < 100 • Presents with headache, fever, cranial nerve paresis, and meningeal irritation • Diagnosis: India ink stain, CALAS
Toxoplasmosis • Cause: Toxoplasma gondii • Transmission: Ingestion of faecally contaminated material, Ingestion of undercooked meat • Risk factor: CD4 < 100 • Asymptomatic in immunocompetent people
Toxoplasmosis • In immunocompromised, mainly involve the CNS • Altered mental status (75%) • Focal neurologic deficits (60%) • Headaches (56%) • Seizures (33%) • Diagnosis: • Serology: IgG and IgM
3rd Hospital Day • Mannitol started • Lumbar puncture done • Opening pressure 120 cmH2O • Clear • WBC 2 Lymphocytes 2 RBC 0 • Sugar 64 (nv 40-75); Protein 47.4 (15-45) • No organisms or pus cells • Negative for AFB, India Ink, KOH, CALAS • Dexamethasone started
4th Hospital Day • X-ray of the left femur – NORMAL • Infectious Diseases referral • History of unprotected sex with multiple sexual partners and bisexual contacts • HIV screening • Whole abdomen UTZ – NORMAL
Multiple Ring Enhancing Lesions on MRI Neoplastic Infectious Primary Metastatic
Multiple Ring Enhancing Lesions on MRI Neoplastic Infectious Bacterial Abscess Tuberculoma Cryptococcus Toxoplasmosis Neurocysticercosis
8th Hospital Day • CD4 count • Serum CALAS • Toxoplasma IgG • Toxoplasma IgM
9th Hospital Day • Discharged, awaiting final report: • Serum CALAS • Toxoplasma IgG • Toxoplasma IgM • CD4 titers and HIV test
Patient Outcome • HIV (+); CD4 = 53 • Toxoplasma IgG 3.8 (nv <2) • Toxoplasma IgM 0.34 (nv <0.5) • Serum CALAS NEGATIVE
Final Diagnosis • Cerebral Toxoplasmosis • HIV infection • Atopic Dermatitis
Management • Toxoplasmosis is rapidly fatal if untreated • Treatment of choice: • Pyrimethamine plus folinic acidplus sulfadiazine • Pyrimethamine plus folinic acid plus clindamycin Danneman et al. Ann Intern Med 1992; 116:33-43. • 6 weeks therapy at least, or until 3 weeks after complete scan resolution • Corticosteroids for raised intracranial pressure Cohn et al. Am J Med 1989; 86: 521-7
Management • Oral co-trimoxazole is effective in doses of 2 tablets 4 times daily for 1 month followed by 2 tablets twice daily as secondary prophylaxis for life • Lifetime prophylactic therapy for toxoplasmosis would only apply if patients are not receiving antiretroviral therapy with the CD4 count being under 200 cells/μl P Francis, January 2004, Vol. 94, No. 1 S Afr Med J