Case Reports in Rheumatology

Volume 2012 (2012), Article ID 640353, 3 pages

doi:10.1155/2012/640353

Case Report

Bilateral Pleural Effusions as an Initial Presentation in Primary Sjögren’s Syndrome

Go Makimoto,1,2 Michiko Asano,¹ Nobukazu Fujimoto,¹ Yasuko Fuchimoto,¹ Katsuichiro Ono,¹ Shinji Ozaki,¹ Koji Taguchi,³ and Takumi Kishimoto¹

¹Department of Respiratory Medicine, Okayama Rosai Hospital, 1-10-25 Chikkomidorimachi, Minami-ku, Okayama 7028055, Japan

²Department of Respiratory Medicine, National Hospital Organization Okayama Medical Center, 1711-1 Tamasu, Kita-ku, Okayama 7011192, Japan

³Department of Pathology, Okayama Rosai Hospital, 1-10-25 Chikkomidorimachi, Minami-ku, Okayama 7028055, Japan

Received 23 August 2012; Accepted 9 October 2012

Academic Editors: P. E. Prete and M. Salazar-Paramo

Copyright © 2012 Go Makimoto et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by sicca symptoms. Interstitial pulmonary fibrosis and tracheobronchial sicca are the most common symptoms of pulmonary involvement in primary SjS, and they are rarely accompanied by serositis such as pleuritis or pericarditis. We report a case of SS presenting initially with bilateral pleural effusions. A 63-year old man was admitted to our hospital with a one-month history of cough, dyspnea, and right chest pain. Chest-computed tomography revealed bilateral pleural effusions. Serum anti-SS-A antibody titer was 1 : 256. Ophthalmological examination revealed a positive Schirmer test. Lip biopsy showed atrophy and plasmacytic infiltration of the salivary gland. Corticosteroid treatment was initiated. Pleural effusions were almost completely resolved by day 30. The patient has not experienced any recurrence.

1. Introduction

Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by sicca symptoms. Pathologically, chronic inflammation is seen in the lacrimal glands and small salivary glands. Interstitial pulmonary fibrosis and tracheobronchial sicca are the most common symptoms of pulmonary involvement in primary SjS, and some cases are also complicated by pulmonary arterial hypertension, pseudolymphoma, pulmonary lymphoma, lymphocytic interstitial pneumonitis, and amyloidosis [1, 2]. However, they are rarely accompanied by serositis such as pleuritis or pericarditis. We report a case of SS presenting initially with bilateral pleural effusions (Table 2).

2. Case Report

A 63-year-old man was admitted to our hospital in December 2011. He had a history of diabetes mellitus, prostate enlargement, and brain infarction. He reported being in his usual state of health until approximately one month earlier, when he developed cough, dyspnea, and right chest pain. He went to a local clinic where computed tomography (CT) of the chest revealed bilateral pleural effusions.

The patient had no fever, rash, joint swelling, or pain. Chest X-ray (Figure 1(a)) and CT (Figure 1(b)) showed bilateral pleural effusions. Laboratory findings on admission were as follows: white blood cells (WBCs) 5700/μL, C-reactive protein (CRP) 9.7 mg/dL, and erythrocyte sedimentation rate (ESR) 100 mm/hr. In addition, the patient was found to be hypothyroid: free thyroxine 4 was 0.59 ng/dL, thyroid stimulating hormone was 48.71 μIU/mL, and antithyroglobulin antibody was over 4000 IU/mL. Pleurocentesis revealed an exudative pleural fluid with no malignant cells but increased proportion of lymphocytes. Protein/albumin concentration and lactase dehydrogenase value in the fluid were 5.6/2.3 g/dL and 315 IU/L, respectively. The smear tests for Mycobacterium tuberculosis and bacterial culture were negative.

(a)

(b)

Figure 1: Chest X-ray (a) and computed tomography (b) showed bilateral pleural effusion without any consolidation or ground glass opacities in the lung.

Antibiotic therapy (tazobactam/piperacillin 4.5 g × 3/day) was initiated and serum CRP decreased to 2.8 mg/dL on the third hospital day. However, the patient developed high fever on the fifth day. Laboratory evaluation for lupus erythematosus was negative, and rheumatoid factor (RF) was 15 IU/L. Serum antinuclear antibody titer was positive at 1 : 320, anti-SS-A antibody titer was positive at 1 : 256, but anti-SS-B antibody was negative. Other antibodies and immunological profile are shown in Table 1. Pleurocentesis was performed; on pleural fluid analysis, antinuclear antibody titer was 1 : 320 and anti-SS-A antibody titer was 1 : 256. Ophthalmological examination revealed a positive Schirmer test. Lip biopsy showed atrophy of the salivary gland and plasmacytic infiltration around the salivary gland ducts (Figure 2), consistent with SS. Ultimately, we diagnosed the patient with SS due to the presence of sicca symptoms. Corticosteroid treatment (prednisolone 40 mg/day) was initiated and produced a drastic decrease in the pleural effusions. Daily prednisolone dose was gradually reduced from 40 mg to 25 mg over three weeks. Pleural effusion was almost completely resolved by day 30. There is no evidence of recurrence thus far.

Table 1: Autoantibody and immunological profile.

Value
Normal value
Unit

Rheumatoid factor
15
0–10
IU/L

IgG
2693
870–1700
mg/dL

IgG4
35.4
4.8–105
mg/dL

IgA
525
110–410
mg/dL

IgM
194
33–190
mg/dL

Antinuclear antibody
X320
<40

Homogenous
X320
—

Speckled
X320
—

Anti-ds-DNA antibody
10
<12
IU/mL

Anticardiolipin antibody (IgM)
1.2
<3.5
IU/mL

Anticardiolipin antibody (IgG)
8
<10
IU/mL

Lupus erythematosus test
Negative
—

Lupus anticoagalant
1.05
<1.3
sec

Preneutralization
32.7
—
sec

Postneutralization
31.2
—
sec

Antiribonucleoprotein

antibody
Negative
—

Anti-Sm antibody
Negative
—

Anti-Sjögren’s syndrome-A antibody
X256
—

Anti-Sjögren’s syndrome-B antibody
Negative
—

Proteinase-3 antineutrophil cytoplasmic antibody
<10
<10
EU

Myeloperoxidase antineutrophil cytoplasmic antibody
<10
<20
EU

Serum complement level
40.8
25–48
CH50/mL

C3
93
86–160
mg/dL

C4
19
17–45
mg/dL

Soluble interleukin 2 receptor
1550
145–519
IU/mL

Table 2: Literature review of primary Sjögren’s syndrome complicated by pleural effusions [3–8].

Authors
Age
Gender
Chief symptoms
ANA
Anti-SS-A
Anti-SS-B

Serum
PE
Serum
PE
Serum
PE

Alvarez-Sala et al.
64
F
Chest pain
+
ND
−
ND
+
ND

Ogihara et al.
62
M
Fever
1 : 40
ND
1 : 4
1 : 4
1 : 8
1 : 8

Suzuki et al.
53
F
Cough
1 : 160
1 : 80
+
ND
+
ND

Kawamata et al.
70
M
Cough
1 : 1280
ND
+
+
−
−

Horita et al.
73
M
Dyspnea
1 : 320
ND
25.9 U/mL
22.3 U/mL
59.1 U/mL
76.4 U/mL

Teshigawara et al.
65
M
Cough, dyspnea
1 : 320
1 : 80
>500 U/mL
89.9 U/mL
49 U/mL
34.3 U/mL

ANA: antinuclear antibody, SS: Sjögren’s syndrome, PE: pleural effusion, ND: not done.

Figure 2: Lip biopsy showed atrophy of the salivary gland and plasmacytic infiltration around the salivary gland ducts.

3. Discussion

In 1989 a European research group proposed classification criterion for SS; this was revised by an American-European consensus group in 2002 [9, 10]. It comprises two subjective criteria, ocular and oral symptoms, four objective criteria including ocular and oral signs, and histopathological and serological findings including antinuclear, anti-SS-A, or anti-SS-B antibodies. The diagnosis of SS requires at least four of the six criteria including histopathological or serological finding, or three of the four objective criteria. Our patient had ocular and oral symptoms and a positive Schirmer test. Furthermore, lip biopsy showed atrophy of the salivary gland with plasmacytic infiltration, and positive antinuclear and anti-SS-A antibodies were detected.

SS is classified into two types: primary and secondary, with the secondary form being complicated by other collagen disorders such as rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and scleroderma. In this case, the patient had no clinical signs of RA or scleroderma. There were some laboratory findings compatible with SLE, but only two criteria of SLE were met: serositis and high titer antinuclear antibody; thus we could not make the diagnosis of SLE. Eventually, a diagnosis of primary SS was reached.

SS is rarely accompanied by pleural effusion. Papathanasiou et al. [11] reported that pleural effusion was observed in no cases of primary SS and in 2 of 26 cases of secondary SS. There have been only six reports of primary SjS complicated by pleural effusion [3–8] (Table 1). Among them, pleural effusion was an initial manifestation only in two cases [6, 8]. Anti-SS-A and/or SS-B antibody was detected in the pleural effusion of these cases. Physicians should take notice to examine these antibodies in undiagnosed pleural effusion.

Corticosteroid therapy, started at 30 or 40 mg/day of prednisolone if not complicated by interstitial pneumonitis, is a common treatment for SS [4]. A good response is expected, but recurrence is also reported during dose reduction [8]. There has been no evidence of recurrence in our patient so far, but careful followup is warranted.

In conclusion, SS should be considered as one of the collagen diseases potentially presenting with pleuritis.

Conflict of Interests

The authors declare that they have no conflict of interests.

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