Sir,
Details of patient history remain important in spite of all technological advancements. Nonneurological symptoms and signs may point to the etiologic diagnosis and should be considered carefully. While diagnostic criteria are helpful, patients’ diseases may sometimes be in a state of evolution and incomplete syndromes also have to be recognized. A nonspecific symptom such as psychosis sometimes gets treated symptomatically without further thought. This may be a missed opportunity to diagnose and provide specific treatment if indicated or at least caution for future events. We present a 44-year-old lady who initially presented with psychosis and later developed an acute polyradiculoneuropathy. She was subsequently found to have probable systemic lupus erythematosus (SLE).
A 44-year-old lady presented with calf pain, paresthesias, and difficulty in getting up from squatting, followed soon by difficulty in climbing upstairs of 2-week duration. Four days later, she developed left facial weakness. On the 10th day, she had limb weakness, which progressed enough to confine her to bed. She had bilateral facial weakness, flaccid areflexic quadriparesis, and an impaired joint position sensation in the right big toe. Her upper limbs were normal with normal bladder and bowel. There was no altered behavior or seizures, upper respiratory tract infection, diarrheal illness, abdominal pain, or cola-colored urine. There were no rashes, photosensitivity, joint pains, or alopecia. A syndromic diagnosis of polyradiculoneuropathy involving the facial nerve as well as spinal nerve roots was made.
Six years ago, she had paranoid delusions, feeling of being watched through a camera with auditory hallucinations which responded to paliperidone that had been continued till date. Three years ago, she was diagnosed with ductal carcinoma of the left breast that was positive for estrogen and progesterone receptors. She was managed with neoadjuvant chemotherapy with docetaxel and epirubicin followed by surgery and chemoradiotherapy.
At presentation, nerve conductions demonstrated a sensorimotor axonal neuropathy in all four limbs. Since the patient had a past history of malignancy, magnetic resonance imaging (MRI) was done to look for carcinomatous infiltration of nerve roots which revealed enhancement along the roots. Cerebrospinal fluid was acellular with raised protein and no malignant cells. Peripheral smear also did not reveal any atypical or leukematous cells. Whole-body positron emission tomography (PET)-computed tomography did not show evidence of disease recurrence.
Keeping in mind her past history of psychosis, a differential diagnosis of porphyria and lupus were also considered. Urine porphyrin was negative whereas antinuclear antibody (ANA) was positive. Extractable nuclear antigen profile revealed anti-Sm, SS-A, and SS-B antibodies. Negative antihistone antibody ruled out drug-induced lupus. Urine analysis showed mild proteinuria (300 mg/24 h). She did not have sicca symptoms such as dryness of mouth and grittiness of eyes. Schirmer's test was done after her facial palsy resolved and was normal [Table 1]. Pleural thickening on PET and ultrasonography chest could have been due to past radiotherapy or pleuritis related to lupus. Table 1 shows her investigation profile in which other systemic involvement of lupus was evaluated.
Table 1.
Investigations and results
| Investigations for localization | Result |
|---|---|
| Nerve conduction study | Bilateral sensorimotor polyneuropathy AMSAN |
| MRI brain | Normal: Enhancement along conus and nerve rootlets |
| MRI Spine | |
| Investigations for etiologic diagnosis | |
| Hemogram | Hb 11.36 TLC 5210 Plt 201510 ESR 20 mm; no atypical cells on peripheral smear |
| Liver/renal functions | U/Cr 31/0.6 Na/K 135/5.5 T.Bil 0.2 SGOT/SGPT 51/46 ALP 71 Alb/Glo 3.3/5 Ca/PO4 8.7/3.4 |
| Chest radiograph | Bilateral reticulonodular shadows |
| Thyroid profile | T3/T4/TSH normal |
| CSF | Acellular, protein 166 mg/dL sugar 71 mg/dL, RBS 104 mg/dL; Gram staining, cryptococcal antigen, GeneXpert negative; malignant cytology no evidence of cancer |
| Serum ACE | 38 U/L (<65) |
| Viral markers | HIV, HBsAg, anti-HCV negative |
| RF, ANCA | Negative |
| Extractable nuclear antigen profile | |
| ANA 1: 640 | Positive |
| Anti-dsDNA | Negative |
| Anti-Sm antibody | Positive |
| U1 Sm/RNP negative | Negative |
| SS-A strong positive +++ | Strong positive +++ |
| Ro 52 strong positive +++ | Strong positive +++ |
| SS-B positive + | Positive + |
| Anti-histone, anti-centromere, anti-SCL-70 IgG, PM-Scl | Negative |
| Anti Jo-1 | Negative |
| PCNA, nucleosome, AMA-M2 antibodies, ribosomal P antibodies | Negative |
| Antiganglioside antibody panel (IgG, IgM) | Negative |
| Urine active sediments | Negative |
| Urine porphyrin screening | Negative |
| Schirmer’s test | 15 mm (>5 mm normal) |
| USG chest | No pleural effusion on either side, bilateral CP angles clear |
| PET-CT | No abnormal uptake |
Ethical clearance: Not required, Patient consent: Obtained. MRI=Magnetic resonance imaging, AMSAN=Acute motor and sensory axonal neuropathy, CSF=Cerebrospinal fluid, ALP=Alkaline phosphatase, TSH=Thyroid-stimulating hormone, ANCA=Antineutrophil cytoplasmic antibodies, RF=Rheumatoid factor, ACE=Angiotensin-converting enzyme, PCNA=Proliferating cell nuclear antigen, PET=Positron emission tomography, CT=Computed tomography, Hb=Hemoglobin, HCV=Hepatitis C virus
On the day of presentation, she was started on intravenous immunoglobulin (IVIg); 125 g was administered over 5 days. While IVIg was being given, and for a week after, it was completed, she continued to worsen. New weakness appeared in the upper limbs. IV methyl prednisolone followed by oral prednisolone was given, and 3 days later, some improvement was noted.
She received monthly cyclophosphamide pulses for 6 months followed by azathioprine 125 mg/day. There were no further relapses and she improved completely.
Peripheral nervous system involvement in lupus is rare. Acute polyradiculoneuropathy has been anecdotally reported in SLE.[1,2,3,4,5] In a cohort of 523 SLE patients, only 1.1% had a Guillain–Barre syndrome-like presentation. Our patient had psychosis in the past. Her magnetic resonance imaging (MRI) brain was normal although neuropsychiatric lupus patients with antibody positivity usually have an abnormal neuroimaging.[6] The patient had ANA, anti-Sm, anti-SS-A, and anti-SS-B positivity. According to the 2015 ACR classification, 4 out of 17 criteria are necessary for a definite diagnosis of SLE. This patient had probable SLE with three criteria: neuropsychiatric manifestations, ANA and anti Sm antibody positivity. She may develop new manifestations over time, or it could be a chance association of the occurrence of multiple diseases such as psychosis, carcinoma of the breast, and acute polyneuropathy. However, the former was likely as antiganglioside antibody panel was negative as well as SLE was a unifying diagnosis, which could explain all her symptoms.
Neuropsychiatric lupus may present with normal MRI brain, and peripheral nervous system involvement can rarely occur in lupus. Paying attention to details can enable early diagnosis and improve outcome by early immunomodulation.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
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Conflicts of interest
There are no conflicts of interest.
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