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Kim and Kong: Relapsing polychondritis presenting with intractable chronic cough, acute visual disturbance, and hearing loss

Relapsing polychondritis presenting with intractable chronic cough, acute visual disturbance, and hearing loss

Hyunje Kim1, Eunjung Kong2
Received April 6, 2025;       Revised June 5, 2025;       Accepted November 19, 2025;
A 61-year-old male was admitted to our hospital following the sudden onset of visual disturbance and hearing difficulty. He experienced an explosive chronic cough that developed after the ocular and auditory symptoms. The cough was refractory to treatment and worsened over several months.
Upon admission, his vital signs were blood pressure 130/70 mmHg, heart rate 109/min, respiratory rate 26/min, and body temperature 37.1°C. Laboratory tests revealed unremarkable serum and urine protein electrophoresis results, except erythrocyte sedimentation rate 73 mm/hr, C-reactive protein 4.27 mg/dL (reference range 0–0.5). Tests for infectious conditions, including blood, sputum, urine, and bronchial washing fluid cultures; tuberculosis interferon-gamma release assay; and serologic tests for bacterial, viral, protozoal, and parasitic agents, were all negative, except for a positive Treponema pallidum hemagglutination assay. Serologic tests for systemic autoimmune diseases and auto-antibodies were negative (Table 1).
Ocular examinations identified panuveitis excluding endophthalmitis, while auditory tests confirmed luetic sensorineural hearing loss. Despite a normal venereal disease research laboratory test, brain MRI/magnetic resonance angiography revealed only small vessel disease without other abnormalities. A cerebrospinal fluid test revealed unremarkable.
To evaluate potential underlying conditions, including lymphoproliferative diseases, malignancies, vasculopathies and hidden infection foci, a positron emission tomography-computed tomography (PET-CT) scan revealed an increased fluorine-18 fluorodeoxyglucose (18-F-FDG) uptake in costal cartilage (Fig. 1B), laryngeal cartilages (Fig. 1A), and tracheal ring cartilage (Fig. 1A), suggesting chondritis.
The patient was diagnosed with relapsing polychondritis, the underlying cause of his intractable chronic cough, alongside panuveitis/endophthalmitis and acute sensorineural hearing loss.
The patient is closely followed at the outpatient department and is currently on methotrexate 12.5 mg weekly, PD 7.5 mg daily, azathioprine 50 mg twice daily, and mycophenolate mofetil 1,000 mg twice daily.
This report details a case of relapsing polychondritis [1], a rare cause of chronic cough without nasal or ear involvement, accompanied by acute uveitis and sensorineural hearing loss.
The study was approved by the Institutional Review Board (IRB) of Yeungnam University Medical Center (IRB No: YUMC 2025-02-030). The IRB waived the requirement for written informed consent from the patient.
Notes
Notes

CRedit authorship contributions

Hyunje Kim: conceptualization, methodology, investigation, data curation, validation, writing - review & editing, visualization; Eunjung Kong: data curation, validation, writing - review & editing, visualization, supervision

Conflicts of Interest
Conflicts of Interest

Conflicts of interest

The authors disclose no conflicts.

Notes
Notes

Funding

None

Figure 1
A coronal PET-CT scan shows FDG uptake in the laryngeal cartilage (A, blue arrows) and trachea (B, white arrowheads), indicating inflammation of the laryngeal and tracheal cartilages. Multiplanar reformation of the PET-CT scan shows FDG uptake in the 2nd to 7th costal cartilages (B, gray arrowheads) consistent with costochondritis. PET-CT, positron emission tomography-computed tomography; FDG, fluorodeoxyglucose.
kjim-2025-112f1.gif
Table 1
Laboratory findings of the case
Laboratory test items Test results Reference range
WBC (/μL) 13.78 4.0–10
Hb (g/dL) 12.4 12–16.5
Platelet (/μL) 430 140–440
ESR (mm/h) 73 0–20
CRP (mg/dL) 4.27 0–0.5
AST (U/L) 21 10–35
ALT (U/L) 35 10–40
BUN (mg/dL) 16.6 8–23
Creatinine (mg/dL) 1.25 0.7–1.2
LDH (U/L) 194 0–250
Albumin (g/dL) 3.08 3.5–5.0
A/G ratio 1.1 1–2.1
IgG (mg/dL) 957 700–1600
HbA1c (%) 6.1 4.4–6.3
MPO-ANCA (U/mL) Negative 0–5
PR3-ANCA (U/mL) Negative 0–5
ANA Negative Negative
RF (IU/mL) 6.3 0–15
ACPA (U/mL) < 8.00 0–16
SS-A Ab (U/mL) Negative 0–15
SS-B Ab (U/mL) Negative 0–15
Scl-70 Ab (Index) Negative Negative
Anti-Jo-1 Ab Negative Negative
Angiotensin-converting enzyme (U/L) 18 13–63
Cryoglobulin Negative Negative

WBC, white blood cell; Hb, hemoglobin; ESR, erythrocyte sedimentation rate; CRP, C-reactive protein; AST, aspartate aminotransferase; ALT, alanine transaminase; BUN, blood urea nitrogen; LDH, lactate dehydrogenase; A/G, albumin/globulin ratio; IgG, immunoglobulin G; HbA1c, glycated hemoglobin; MPO-ANCA, myeloperoxidase-specific antineutrophil cytoplasmic antibody; PR3-ANCA, proteinase 3-specific antineutrophil cytoplasmic antibody; ANA, antinuclear antibody; RF, rheumatoid factor; ACPA, anti-citrullinated peptide antibodies; SS-A, anti-Sjogren’s syndrome-related antigen A autoantibodies; SS-B, anti-Sjogren's syndrome-related antigen B autoantibodies; Scl-70 Ab, antitopoisomerase-1 antibody.

References
References

REFERENCE

1. Kingdon J, Roscamp J, Sangle S, D’Cruz D. Relapsing polychondritis: a clinical review for rheumatologists. Rheumatology (Oxford) 2018;57:1525–1532.
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