CASE REPORT
Laryngeal Involvement in Systemic Lupus Erythematosus
Report of Two Cases
K. Murat Ozcan, MD,* Secil Bahar, MD,* Ibrahim Ozcan, MD,* Lale Pasaoglu, MD,†
Engin Sennaroglu, MD,‡ Yasar Karaaslan, MD,§ and Huseyin Dere, MD*
Abstract: Systemic lupus erythematosus is a multisystem autoim-
mune disorder. Joint and skin involvements are the most frequent
presenting features. Laryngeal involvement, however, is extremely
rare. Symptoms of laryngeal involvement may range from mild hoarse-
ness to life-threatening respiratory distress. In this article, 2 patients
with systemic lupus erythematosus and laryngeal involvement are
presented. The first patient had hoarseness and noisy respiration, and
the second had cough and respiratory distress. Otorhinolaryngological
examination revealed laryngeal inflammation in both. Our cases re-
sponded well to systemic corticosteroids. Patients with symptoms such
as hoarseness, foreign body sensation in throat, and respiratory distress
should be evaluated by an otorhinolaryngologist to rule out involvement
of the laryngeal structures.
Key Words: systemic lupus erythematosus, larynx, joints
(J Clin Rheumatol 2007;13: 278 –279)
S
ystemic lupus erythematosus (SLE) is a multisystem disor-
der that is characterized by inflammation induced by auto-
antibodies.
1
Arthritis, pleuritis, pericarditis, nephritis, and central
nervous system involvement are common. Although relatively
common in rheumatoid arthritis, laryngeal involvement is rare
in SLE.
In this article, 2 patients with laryngeal manifestations
of SLE are presented, and the literature is reviewed.
CASE REPORT
Case 1
A 25-year-old woman with SLE was consulted to an
otorhinolaryngology clinic due to hoarseness, noisy respira-
tion, and foreign body sensation in her throat. She was
diagnosed as SLE by the clinic of rheumatology 5 years ago
and was under routine follow-up. She had nephritis, pleuritis,
and skin involvement at the time of diagnosis. She had no
clinical signs of Sjogren syndrome. Systemic corticosteroids
and chloroquine were administered for 4 years and then
chloroquine was stopped. She was already on 20 mg/d pred-
nisolone. Her first laryngeal symptom was hoarseness and
appeared 3 weeks before the visit. Later she had noisy
respiration and foreign body sensation in her throat. In her
otorhinolaryngological examination, there was no ulceration
or other lesions in her oropharynx. In videolaryngostrobo-
scopic (VLS) examination, the mucosa overlying the aryte-
noids was red and thickened, and the movements of both
arytenoids were limited in inspiration and phonation. Bowing
was evident in her true vocal folds. Laryngeal computerized
tomography (CT) revealed thickening in the aryepiglottic fold
and asymmetry of arytenoids (Fig. 1). In laboratory exami-
nation, blood sedimentation rate was 71 mm/h (6.00 –15.00),
CRP was 27.8 mg/L (0.00 –5.00), leukocytes: 4.94 K/L
(4.40 –11.30), hematocrit 36.6% (37.7–53.7), total protein: 66
g/L (64 – 83) ALT: 12 U/L (5– 40), AST: 21 U/L (5– 42),
direct Coombs test: negative, ANA: positive, anti-DNA:
negative, C3: 1.51 g/L (0.90 –1.80), C4: 0.184 g/L (0.10 –
0.40), SSA and SSB-negative. Systemic corticosteroid dose
was increased (prednisolone, 1 mg/kg/d, p.o.), and she in-
haled cold steam regularly. Her symptoms regressed in a
period of 2 weeks.
After treatment, VLS examination was normal except
for bowing of the true vocal folds. She is under follow-up
since 12 months and has no laryngeal symptoms.
Case 2
A 24-year-old woman with a recent diagnosis of SLE and
symptoms of hoarseness, foreign body sensation in throat,
cough, and respiratory distress for 2 days was consulted to the
otorhinolaryngology clinic. In laboratory examination, her blood
sedimentation rate was 37 mm/h (6.00 –15.00), CRP: 141 mg/L
(0.00 –5.00), RF: 9.88 IU/mL (0.00 –15.00), Leukocyte count:
10.5 K/L (4.40 –11.30), hematocrit: 29% (37.7–53.7), total
protein: 73 g/L (64 – 83), ALT: 13 U/L (5– 40), AST: 25 U/L
(5– 42), ANA: positive, anti-DNA: negative, C3: 0.75 g/L
(0.90 –1.80), and C4: 0.07 g/L (0.10 – 0.40). She was recently
diagnosed as SLE with nephritis and central nervous system
involvement. She has no sicca symptoms. In otorhinolaryngo-
logical examination, there was no ulceration or other lesions in
her oropharynx. In VLS examination, the mucosa overlying the
arytenoids was red and thickened. The arytenoids seemed asym-
metric. In laryngeal CT, the right true vocal fold seemed thick-
From the *4th ENT Clinic, †Department of Radiodiagnostics, ‡Clinic of
Rheumatology, and §Clinic of Internal Medicine, Ankara Numune
Education and Research Hospital, Ankara, Turkey.
Reprints: K. Murat Ozcan, MD, Yucetepe sit. A blok. 59/6 06580 Anittepe,
Ankara, Turkey. E-mail: kursatmuratozcan@yahoo.com.
Copyright © 2007 by Lippincott Williams & Wilkins
ISSN: 1076-1608/07/1305-0278
DOI: 10.1097/RHU.0b013e318157f25e
JCR: Journal of Clinical Rheumatology • Volume 13, Number 5, October 2007 278