Methimazole associated eosinophilic pleural effusion: a case report
© The Author(s). 2017
Received: 2 December 2016
Accepted: 28 January 2017
Published: 21 March 2017
Adverse reactions associated to anti-thyroid drugs include fever, rash, arthralgia, agranulocytosis and hepatitis that are thought to be hypersensitivity reactions. Five cases of pleural effusion associated to thionamides have also been reported, two with propylthiouracil and three with carbimazole.
We report here a case of a 75-year-old man admitted because of unilateral pleural effusion. The patient had a recent diagnosis of hyperthyroidism and 6 days after starting methimazole complained of pleuritic chest pain. He had elevated C-reactive protein and erythrocyte sedimentation rate and normal white blood cell count and liver enzymes. Chest radiography showed a moderate right pleural effusion and the ultrasound revealed a loculated effusion that was shown to be an eosinophilic exudate.
The temporal relationship between methimazole intake and the development of pleural effusion combined with the extensive exclusion of alternative causes, namely infectious, neoplastic and primary auto-immune diseases, led to the diagnosis of hypersensitivity reaction to methimazole. The thionamide was stopped and corticosteroid was started with complete resolution of the pleural effusion in 3 months.
Awareness of this rare adverse reaction of anti-thyroid drugs is important and methimazole can be added to the list of possible etiologies of drug-induced eosinophilic pleural effusion.
KeywordsEosinophilic pleural effusion Thionamides Methimazole Hypersensitivity reaction Case report
Methimazole or thiamazole, together with carbimazole and propylthiouracil, are anti-thyroid medications belonging to the class of thionamides . Methimazole is the active metabolite of carbimazole and has similar pharmacological activity. Thionamides side effects are rare and include fever, rash, arthralgias, agranulocytosis and hepatitis . Pleuro-pulmonary complications of these drugs are even rarer.
The mechanisms of thionamides side effects are poorly understood but are generally considered to be dose independent by immunologic hypersensitivity. Antineutrophil cytoplasmic antibody (ANCA)-positive vasculitis associated to anti-thyroid drugs have been well described [2–12]. Additionally, a drug-induced lupus-like syndrome and hypersensitivity reactions with cutaneous, renal or pulmonary involvement have also been identified [13–17]. Recently, five cases of pleural effusion induced by anti-thyroid drugs, two with propylthiouracil and three with carbimazole, have been reported in the literature [18–22].
We describe here a patient with hyperthyroidism who developed an unilateral eosinophilic pleural effusion a few days after the initiation of methimazole therapy. An extensive diagnostic evaluation excluded infectious and neoplastic diseases as well as primary auto-immune or vasculitic disease as the cause of serositis. Pleural effusion was thus considered as a manifestation of methimazole-hypersensitivity reaction. To the best of our knowledge, this is the first case of methimazole-induced pleural effusion described in the literature.
A 75-year-old man was admitted with unilateral right pleural effusion. He presented with pleuritic chest pain that started 4 days before and had no other relevant complaints, namely fever, diaphoresis, dyspnoea, cough, haemoptysis, rash or arthralgia.
He had a past medical history of arterial hypertension, atrial fibrillation, end-stage renal disease on haemodialysis, peripheral artery disease and prostatic hyperplasia. His ambulatory prescription consisted of enalapril, carvedilol, nifedipine, aspirin, warfarin, omeprazole and tansulosin, for more than 3 years. Amiodarone had been suspended, 2 months before, due to ocular toxicity. There was no evidence of thoracic trauma or previous asbestos exposure.
Ten days before hospital admission the patient had an episode of unstable angina. He underwent coronary angiography which showed a lesion in the circumflex artery and angioplasty and implantation of an intracoronary stent coated drug were performed. He started treatment with clopidogrel. By this time blood tests showed low TSH (0.055 uU/mL; reference range: 0.55–4.78 uU/mL) and high FT4 (1.81 ng/dL; reference range: 0.80–1.76 ng/dL) and FT3 (4.84 pg/mL; reference range: 2.3–4.2 pg/mL). Methimazole was started. There was no evidence of pleural effusion at that time.
At hospital admission the patient was afebrile, with a respiratory rate of 18 cycles per minute and oxygen saturation of 95% on room air. His blood pressure was 131/63 mmHg and heart rate was 76 beats per minute. Cardio-pulmonary examination revealed arrhythmic heart sounds, diminished breath sounds on the lower half of the right lung and dullness on percussion at that site was noted. All other findings on physical examination were unremarkable.
Laboratory tests showed normal leucocytes (6 510/uL) and eosinophils (320/uL) counts, elevated C-reactive protein (10.9 mg/dL) and erythrocyte sedimentation rate (58 mm) and normal liver enzymes; TSH (0.019 uU/mL) was low and FT4 (2.51 ng/dL) and FT3 (7.22 pg/mL) were high; INR (1.13) was not in therapeutic range. Arterial blood gases, while the patient was in room air and after haemodialysis, showed hypoxemia (PO2: 57.6 mmHg) and metabolic alkalosis (pH: 7.48, PCO2: 37.8 mmHg, HCO3 −: 28.9 mmol/L). Electrocardiogram revealed atrial fibrillation rhythm without acute ischaemic changes. Chest radiography showed a homogenous opacity in the lower half of the right pulmonary field and chest ultrasound findings were suggestive of pleural effusion with septa. Right-sided diagnostic thoracentesis was performed. The aspirated pleural fluid had 2277 cells/uL with 70% being macrophages, 18% eosinophils and 12% neutrophils. The effusion protein/serum protein ratio was 0.7 and the effusion lactate dehydrogenase (LDH)/serum LDH ratio was 1.8. Pleural fluid cultures revealed no bacteria or mycobacteria and no malignant cells were detected on cytological examination of pleural fluid. Bronchofibroscopy did not reveal any macroscopic lesion. Bronchoalveolar fluid cultures were negative and the cytological analysis of the fluid showed no malignant cells. Pleural biopsy was not performed due to high bleeding risk as the patient was on double anti-platelet and anticoagulation therapy. The blood cultures yielded no bacteria or mycobacteria and blood interferon gamma release assay for Mycobacterium tuberculosis was negative. Anti-nuclear antibodies (ANA), anti-double stranded DNA (anti-dsDNA) antibodies and ANCA were negative.
Thoracic, abdominal and pelvic computed tomography (CT) was performed and confirmed the moderate right pleural effusion with no other positive findings. Thoracic CT angiography excluded pulmonary embolism. Although Dressler syndrome was considered , it usually occurs after myocardial infarction rather than unstable angina and moreover, the short interval between the cardiac event and the pleural effusion did not support this hypothesis .
Titers of thyroglobulin (Tg), anti-Tg, anti-thyroperoxidase and anti-TSH receptor antibodies were normal. The cervical ultrasonography revealed thyroid micronodules and there was no radioisotope uptake in the 99mTechnetium thyroid scintigraphy. Hyperthyroidism was interpreted as type II amiodarone induced thyrotoxicosis.
After the exclusion of neoplastic, infectious and primary auto-immune diseases, considering an exudative pleural effusion with significant eosinophilia and a well-established temporal relation with the initiation of methimazole treatment, a diagnosis of methimazole-induced pleural effusion was made. A single organ drug hypersensitivity reaction was assumed in the absence of evidence of other organ involvement. Anti-thyroid medication was suspended, systemic corticosteroid was initiated and all other medications were maintained. Progressive and rapid clinical and laboratorial improvement was evident with normalization of inflammatory biomarkers and thyroid function and resolution of hypoxemia. Three months after methimazole was suspended there was complete resolution of pleural effusion.
Thionamides-induced auto-immune phenomena, including pleuro-pulmonary complications, exhibit usually the features of ANCA-positive systemic vasculitis. Stankus et al. published, in 1992, the first case of propylthiouracil-induced hypersensitivity vasculitis and since then 61 cases of vasculitis associated to anti-thyroid drugs have been reported, most involving propylthiouracil [15, 25]. There are only nine reported cases of carbimazole-induced vasculitis and seven cases of vasculitis associated to methimazole [2–9, 13, 14, 17, 25–29]. In addition, a lupus-like syndrome can be induced by any of the thionamides [8, 13, 14, 21, 30]. Clinical manifestations are similar to systemic lupus erythematosus (SLE) and usually patients have positive anti-nuclear, anti-dsDNA and anti-histone antibodies .
Pleuro-pulmonary complications of thionamides are very rare and include alveolar hemorrhage, interstitial pneumonia, pulmonary cavitations and pleural effusion that are considered adverse auto-immune reactions triggered by these drugs [6, 7, 9, 18–22, 31, 32]. Five cases of anti-thyroid drug-induced pleural effusion, two with propylthiouracil and three with carbimazole, have been described in the literature [18–22]. The case reported here represents the first case of methimazole-associated pleural effusion. The temporal relationship between initiation of the drug and the appearance of pleural effusion, the resolution of the effusion after withdrawal of methimazole with administration of corticosteroid, in the absence of other potential cause for pleuritis, is consistent with the diagnosis of drug-induced pleural effusion. Our case differs from the previous reports by the short time between the initiation of the thionamide and the onset of pleural effusion that was only 6 days.
Pleural fluid of the two patients with propylthiouracil associated pleuritis was an eosinophilic exsudate, as in the case reported here [18, 19]. Pleural biopsy was made in one of these patients and showed chronic inflammation of the pleura with prominent eosinophils and both patients had negative auto-immune markers. None of the three patients with carbimazole-induced pleuritis had an eosinophilic exudate [20–22]. Two of these three reported cases had pleural nonspecific inflammatory infiltrates and negative auto-immunity, namely ANA and ANCA. The third patient had positive ANA, anti-dsDNA and anti-histone antibodies and pleuritis was considered as a drug-induced SLE-like syndrome.
As stated before, the mechanisms involved in these cases are most likely non-dose dependent, exactly like in drug induced liver injury where lesions occur via immunologic hypersensitivity  by generation of toxic metabolites  or alternatively metabolites that induce an immunological reaction [34, 35]. The inflammatory response with abundant eosinophils in the case reported here suggests that this represents a T cell drug hypersensitivity reaction with polarization to T helper 2 cells producing interleukin 4 and interleukin 5 that are known to induce eosinophil differentiation. Interestingly, a recent report by Uematsu et al. , identified a T helper 2 biased lymphocyte response in a model of methimazole acute liver injury mediated by microRNAs . Another area of increasing interest is that of risk factors for methimazole adverse reactions. Thus, HLA-B*27:05 and other single nucleotide polymorphisms were identified as possible risk factors for anti-thyroid agranulocytosis , and the prospect that certain microRNAs with effects on lung development might represent prognostic tools in thyroid-dependent lung disease  has also been recently discussed.
The clinical and radiological evolution of this case was identical to the cases of pleural effusion induced by other thionamides. The anti-thyroid drug considered to be associated to the effusion was withdrawn in all patients and alternative anti-thyroid therapy options were initiated in three of the five patients [19, 20, 22]. The cessation of the drug was followed by resolution of the effusion within 3 to 5 months. Two of the five patients were given corticoesteroid for a short period of time and in decreasing dosages and in these cases a more rapid resolution of serositis was observed [19, 21]. In the present case, a diagnosis of type II hyperthyroidism, due to cytotoxic effect of amiodarone on thyroid cells, was made and thus maintenance of thionamides treatment was not required.
In conclusion, we describe here the first case of eosinophilic pleuritis associated to methimazole due to an hypersensitivity immune drug reaction with full remission after withdrawal the drug. Awareness of clinicians about the possibility of this drug adverse reaction may help identification of future similar cases.
Antineutrophil cytoplasmic antibody
Anti-double stranded DNA antibodies
Systemic lupus erythematosus
The authors would like to thank the patient for granting consent for publication.
This report received no research funding.
Availability of data and materials
The data that support the findings of this case are included in this published article.
PGC, JH, SV, SB and JMS analyzed and interpreted the present case and were involved in the diagnostic approach; PGC, FDS, JH, SV, SB, JMS and RMMV did a review of the literature; PGC, FDS and SB wrote a first draft. PGC, SB, SV, JMS and RMMV finalized the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report. A copy of the written consent is available for review by the editor of this journal.
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- Cooper DS. Antithyroid drugs. N Engl J Med. 2005;352:905–17.View ArticlePubMedGoogle Scholar
- D’Cruz D, Chesser AM, Lightowler C, Comer M, Hurst MJ, Baker LR, Raine AE. Antineutrophil cytoplasmic antibody-positive glomerulonephritis associated with anti-thyroid drug treatment. Br J Rheumatol. 1995;34:1090–1.View ArticlePubMedGoogle Scholar
- Hori Y, Arizono K, Hara S, Kawai R, Hara M, Yamada A. Antineutrophil cytoplasmic antibodies-positive crescentic glomerulonephritis associated with thiamazole therapy. Nephron. 1996;74:734–5.View ArticlePubMedGoogle Scholar
- Miller RM, Savige J, Nassis L, Cominos BI. Antineutrophil cytoplasmic antibody (ANCA)-positive cutaneous leucocytoclastic vasculitis associated with antithyroid therapy in Graves’disease. Australas J Dermatol. 1998;39:96–9.View ArticlePubMedGoogle Scholar
- Gunton JE, Stiel J, Caterson RJ, McElduff A. Anti-thyroid drugs and anti-neutrophil antibody positive vasculitis. A case report and review of the literature. J Clin Endocrinol Metab. 1999;84:13–6.View ArticlePubMedGoogle Scholar
- Tsai MH, Chang YL, Wu WC, Chang CC, Huang TS. Methimazole-induced pulmonary hemorrhage associated with antimyeloperoxidase-antineutrophil cytoplasmic antibody: a case report. J Formos Med Assoc. 2001;100:772–5.PubMedGoogle Scholar
- Calañas-Continente A, Espinosa M, Manzano-García G. Necrotizing glomerulonephritis and pulmonary hemorrhage associated with carbimazole therapy. Thyroid. 2005;15:286–8.View ArticlePubMedGoogle Scholar
- Mehndiratta MM, Pandey S, Kushwaha RS, Mehndiratta P. Carbimazole induced ANCA positive vasculitis. J Assoc Physicians India. 2008;56:801–3.PubMedGoogle Scholar
- Lau EYF, So S, Chan E, Kwok J, Ma J, Kung Annie WC. Methimazole-induced antineutrophil cytoplasmic antibody-associated diffuse alveolar haemorrhage in a chinese woman with Graves’ disease. Hong Kong Med J. 2009;15:209–12.PubMedGoogle Scholar
- Sera N, Ashizawa K, Ando T, Abe Y, Ide A, Usa T, Tominaga T, Ejima E, Yokoyama N, Eguchi K. Treatment with propylthiouracil is associated with appearance of antineutrophil cytoplasmic antibodies in some patients with Graves’ disease. Thyroid. 2000;10:595–9.View ArticlePubMedGoogle Scholar
- Gunton JE, Stiel J, Clifton-Bligh P, Wilmshurst E, McElduff A. Prevalence of positive anti-neutrophil cytoplasmic antibody (ANCA) in patients receiving anti-thyroid medication. Eur J Endocrinol. 2000;142:587–90.View ArticlePubMedGoogle Scholar
- Wada N, Mukai M, Kohno M, Notoya A, Ito T, Yoshioka N. Prevalence of serum anti-myeloperoxidase antineutrophil cytoplasmic antibodies (MPO-ANCA) in patients with Graves’ disease treated with propylthiouracil and thiamazole. Endocr J. 2002;49(3):329–34.View ArticlePubMedGoogle Scholar
- Kawachi Y, Nukaga H, Hoshino M, Iwata M, Otsuka F. ANCA-associated vasculitis and lupus-like syndrome caused by methimazole. Clin Exp Dermatol. 1995;20:345–7.View ArticlePubMedGoogle Scholar
- Thong HY, Chu CY, Chiu HC. Methimazole-induced anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis and lupus-like syndrome with a cutaneous feature of vesiculo-bullous systemic lupus erythematosus. Acta Dermato Venereologica. 2002;82:206–8.View ArticlePubMedGoogle Scholar
- Stankus SJ, Johnson NT. Propylthiouracil-induced hypersensitivity vasculitis presenting as respiratory failure. Chest. 1992;102:1595–6.View ArticlePubMedGoogle Scholar
- Chastain MA, Russo GG, Boh EE, Chastain JB, Flabella A, Milikan LE. Propylthiouracil hypersensitivity: report of two patients with vasculitis and review of the literature. J Am Acad Dermatol. 1999;41(5):757–64.View ArticlePubMedGoogle Scholar
- Day C, Bridger J, Rylance P, Jackson M, Nicholas J, Odum J. Leukocytoclastic vasculitis and intersticial nephritis with carbimazole treatment. Nephrol Dial Transplant. 2003;18:429–31.View ArticlePubMedGoogle Scholar
- Middleton KL, Santella R, Couser Jr JI. Eosinophilic pleuritis due to propylthiouracil. Chest. 1993;103:955–6.View ArticlePubMedGoogle Scholar
- Sen N, Ermis H, Karatasli M, Habesoglu MA, Eyuboglu FO. Propylthiouracil-associated eosinophilic pleural effusion: a case report. Respiration. 2007;74:703–5.View ArticlePubMedGoogle Scholar
- Das G, Stanaway SERS, Brohan L. Carbimazole induced pleural effusion: a case report. Case Reports Endocrinol. 2012. doi:10.1155/2012/941241.Google Scholar
- Haq I, Sosin MD, Wharton S, Gupta A. Carbimazole-induced lupus. BMJ Case Reports. 2013. doi:10.1136/bcr-2012-007596.Google Scholar
- Attard CDC, Gruppetta M, Vassallo J, Vella S. Carbimazole-induced exsudative pleural effusions. BMJ Case Reports. 2016. doi:10.1136/bcr-2016-215080.Google Scholar
- Bielsa S, Corral E, Bagüeste P, Porcel JM. Characteristics of pleural effusions in acute idiopathic pericarditis and post-cardiac injury syndrome. Ann Am Thorac Soc. 2016;13(2):298–300. doi:10.1513/AnnalsATS.201510-668LE.PubMedGoogle Scholar
- Seizner TJ, King Jr TE, Antony VB, Sahn SA. The pleuropulmonary manifestations of the postcardiac injury syndrome. Chest. 1983;84:383–7.View ArticleGoogle Scholar
- Sève P, Stankovic K, Michalet V, Vial T, Scoazec J-Y, Broussolle C. Carbimazole induced eosinophilic granulomatous vasculitis localized to the stomach. J Intern Med. 2005;258:191–5.View ArticlePubMedGoogle Scholar
- Leger JM, Dancea S, Brunet P, Hauw JJ. Polineuropathy during treatment with carbimazole. Rev Neurol. 1984;140:652–6.PubMedGoogle Scholar
- Pasquier E, Genereau T, Baudrimont M, Cabane J, Biour M, Imbert JC. Biopsy-proven myositis with microvasculitis in association with carbimazole. Lancet. 1991;338:1082–3.View ArticlePubMedGoogle Scholar
- Yazbeck R, Francoual J, Benoit P, Tauveron I, Tchen C, Thieblot P. Carbimazole and leucocytoclastic vasculitis: a propos of a case. Revue Medicine Interne. 1999;20:350–2.View ArticleGoogle Scholar
- Rahman MU, Fan C-M, Choi HK. Case 30-2001 - A 22-year-old man with hyperthyroidism, fever, abdominal pain, and arthralgia. N Engl J Med. 2001;345:981–6.View ArticleGoogle Scholar
- Horton RC, Sheppard MC, Emery P. Propylthiouracil-induced systemic lupus erythematosus. Lancet. 1989;2:568.View ArticlePubMedGoogle Scholar
- Miyazono K, Okasaki T, Uchida S, Totsuka Y, Matsumoto T, Ogata E, Terakawa K, Kurihara N, Takeda T. Propylthiouracil-induced diffuse interstitial pneumonia. Arch Intern Med. 1984;144:1764–5.View ArticlePubMedGoogle Scholar
- Cassorla FG, Finegold DN, Parks JS, Tenore A, Thawerani H, Baker L. Vasculitis, pulmonary cavitation, and anemia during anti-thyroid drug therapy. Am J Dis Childhood. 1983;137:118–22.Google Scholar
- Maria VA, Victorino RM. Diagnostic value of specific T cell reactivity to drugs in 95 cases of drug induced liver injury. Gut. 1997;41(4):534–40.View ArticlePubMedPubMed CentralGoogle Scholar
- Tarantino G, Di Minno MN, Capone D. Drug-induced liver injury: is it somehow foreseeable? World J Gastroenterol. 2009;15(23):2817–33.View ArticlePubMedPubMed CentralGoogle Scholar
- Maria VA, Pinto L, Victorino RM. Lymphocyte reactivity to ex-vivo drug antigens in drug-induced hepatitis. J Hepatol. 1994;21(2):151–8.View ArticlePubMedGoogle Scholar
- Uematsu Y, Akai S, Tochitani T, Oda S, Yamada T, Yokoi T. MicroRNA-mediated Th2 bias in methimazole-induced acute liver injury in mice. Toxicol Appl Pharmacol. 2016;307:1–9. doi:10.1016/j.taap.2016.07.008. Epub 2016 Jul 12.View ArticlePubMedGoogle Scholar
- Hallberg P, Eriksson N, Ibañez L, Bondon-Guitton E, Kreutz R, Carvajal A, et al. Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population. Lancet Diabetes Endocrinol. 2016;4(6):507–16. doi:10.1016/S2213-8587(16)00113-3. Epub 2016 May 3.View ArticlePubMedGoogle Scholar
- Bjørnstad S, Samara A, Erichsen A, Paulsen RE, Glover JC, Roald B. Hampered lung maturation in methimazole-induced hypothyroidism in fetal chicken: morphological and molecular correlates to human fetal development. Neonatology. 2016;110(2):83–92. doi:10.1159/000444656. Epub 2016 Apr 13.View ArticlePubMedGoogle Scholar