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Introduction Propylthiouracil (PTU) belongs to thionamide group of a drug, which is used as first line drug in the management of hyperthyroidism. Side effects caused by PTU vary from nonspecific signs and symptoms such as pruritis, urticaria, myalgia, drug-induced fever, and generalized maculopapular rashes to severe side effects such as agranulocytosis, thrombocytopenia, vasculitis, pancreatitis, nephrotic syndrome, and hepatitis.[12] Pulmonary complications like adults respiratory distress syndrome and interstitial pneumonia are extremely rare.[34] We report a case of hemoptysis/alveolar hemorrhage in a patient with hyperthyroidism who was on treatment with PTU. Case Report This is a case report of 24-year-old female, known the case of hyperthyroidism since 4 years. Patient came to our emergency department with a history of fever and myalgia since 3 days and coughing out of blood since 1 day. Patient was taking PTU (100 mg/day) since 4 years. There was no history of any use of anticoagulants or antiplatelets.

of 24-year-old female, known the case of hyperthyroidism since 4 years. Patient came to our emergency department with a history of fever and myalgia since 3 days and coughing out of blood since 1 day. Patient was taking PTU (100 mg/day) since 4 years. There was no history of any use of anticoagulants or antiplatelets. In the emergency department patient was conscious, febrile, tachypnoic, pulse rate - 120 beats/min, blood pressure - 100/60 mmHg, SpO2 -91% with face mask 10 L of oxygen, GRBS - 112 mg/dl, and on auscultation bilateral coarse crepitation were heard. Arterial blood gas analysis showed pH - 7.125, PO2 - 52.2, PCO2 - 63, and HCO3 - 20.2. Patient was immediately intubated and given positive pressure ventilation in view tachypnea, hypotension, and type-II respiratory failure. Complete blood picture showed hemoglobin - 6.9 g/dl, white blood cell of 3200 cells/cumm (neutrophils - 73%), platelets - 1.65 lakhs/cumm, erythrocyte sedimentation rate - 53 mm/h. Prothrombin time 13.5 s (control 11–14 s), INR - 1.51, and activated partial thromboplastin time - 25.4 s (control 30–40 s). Serum electrolytes, liver function test, and kidney function test were normal. Routine urine analysis showed plenty of red blood cells. Electrocardiogram showing sinus tachycardia and two-dimensional-echo showed no regional wall motion abnormality with good left ventricular function.

in time - 25.4 s (control 30–40 s). Serum electrolytes, liver function test, and kidney function test were normal. Routine urine analysis showed plenty of red blood cells. Electrocardiogram showing sinus tachycardia and two-dimensional-echo showed no regional wall motion abnormality with good left ventricular function. Chest X-ray showed [Figure 1] bilateral homogenous opacities. Thyroid function tests were normal. Chest computed tomography showed [Figure 2] diffuse multifocal patchy areas of consolidation and ground glassing in both lungs (alveolar hemorrhage). Venous Doppler of both legs was normal. Bronchoalveolar lavage (BAL) showed hemosiderin-laden macrophages. Culture of BAL fluid and blood was negative for bacteria, tuberculosis, and fungus. Serum antinuclear antibodies (ANA) +ve, anti-dsDNA −ve, anti-histone antibody +ve, p-ANCA +ve, c-ANCA −ve, and anti-GBM −ve with low C3 and C4. Figure 1 Chest X-ray showing bilateral haziness all over the lung fields Figure 2 Computed tomography scan chest (plain) showing diffuse multifocal patchy areas of consolidation and ground glassing in both lungs

Chest X-ray showed [Figure 1] bilateral homogenous opacities. Thyroid function tests were normal. Chest computed tomography showed [Figure 2] diffuse multifocal patchy areas of consolidation and ground glassing in both lungs (alveolar hemorrhage). Venous Doppler of both legs was normal. Bronchoalveolar lavage (BAL) showed hemosiderin-laden macrophages. Culture of BAL fluid and blood was negative for bacteria, tuberculosis, and fungus. Serum antinuclear antibodies (ANA) +ve, anti-dsDNA −ve, anti-histone antibody +ve, p-ANCA +ve, c-ANCA −ve, and anti-GBM −ve with low C3 and C4. Figure 1 Chest X-ray showing bilateral haziness all over the lung fields Figure 2 Computed tomography scan chest (plain) showing diffuse multifocal patchy areas of consolidation and ground glassing in both lungs In view of above features, we suspected PTU-induced autoimmune disease (drug-induced lupus [DIL] and/vasculitis) and hence PTU was stopped. Treated with methylprednisolone (1 g) pulse therapy for 3 days followed by one dose of cyclophosphamide (750 mg). Image-3 showing chest X-ray during the recovery phase (after cyclophosphamide therapy) with a bilateral clearance of haziness. Received one unit of packed red blood cell's during the stay. Clinical features and laboratory parameters improved over a period of 8 days and patient could be extubated on 8 th day and gradually weaned from BIPAP support to nasal prongs, later shifted to room and discharged home successfully on day 12. Figure 3 showing chest X-ray of the same patient before discharge. Figure 3 Chest X-ray of the same patient before discharge

In view of above features, we suspected PTU-induced autoimmune disease (drug-induced lupus [DIL] and/vasculitis) and hence PTU was stopped. Treated with methylprednisolone (1 g) pulse therapy for 3 days followed by one dose of cyclophosphamide (750 mg). Image-3 showing chest X-ray during the recovery phase (after cyclophosphamide therapy) with a bilateral clearance of haziness. Received one unit of packed red blood cell's during the stay. Clinical features and laboratory parameters improved over a period of 8 days and patient could be extubated on 8 th day and gradually weaned from BIPAP support to nasal prongs, later shifted to room and discharged home successfully on day 12. Figure 3 showing chest X-ray of the same patient before discharge. Figure 3 Chest X-ray of the same patient before discharge Discussion Hyperthyroidism is a condition characterize by excessive production of thyroid hormones. It is common in women than men (5:1 ratio) with an overall prevalence of approximately 1.3%.[5] PTU is commonly used as first line drug in the management of hyperthyroidism. PTU inhibits the synthesis of thyroid hormones by blocking the oxidation of iodine in the thyroid gland. PTU can induce adverse autoimmune responses such as DIL or vasculitis.[6] The risk of developing DIL with using PTU is <1% of the treated patients.[7] Patients with PTU-induced DIL have more serositis, musculoskeletal, and gastrointestinal involvement with positive ANA, anti-DNA, and anti-histone antibodies, whereas the ANCA-associated vasculitis will present with upper airway, pulmonary, and renal involvement with c-ANCA positive.[8] Our patient had positive for anti-histone antibodies which suggest DIL and positive p-ANCA with lung (alveolar hemorrhage) and renal involvement (hematuria) show features of vasculitis.

dies, whereas the ANCA-associated vasculitis will present with upper airway, pulmonary, and renal involvement with c-ANCA positive.[8] Our patient had positive for anti-histone antibodies which suggest DIL and positive p-ANCA with lung (alveolar hemorrhage) and renal involvement (hematuria) show features of vasculitis. PTU-induced vasculitis often occurs in a few weeks to years after starting the treatment. Our patient was on PTU treatment since 4 years. The disorder is not dose-dependent and usually improves after discontinuation of the drug,[9] while about 50% of PTU-induced vasculitis need steroids or immunosuppressive drugs.[10] The proposed mechanism for PTU-induced vasculitis is due to the interaction between PTU and neutrophil myeloperoxidase (MPO). MPO and hydrogen peroxide produced by neutrophils can metabolize the drug leading to the reactive intermediates that are immunogenic for T-cells and stimulate the immune system.[11] This case report mainly emphasizes to have a high suspicion for the occurrence of the drug-induced autoimmune disorder in patients with hyperthyroidism treated with PTU. Early diagnosis and treatment with immunosuppressants agents along with supportive care and withdrawal of the drug can make a difference in morbidity and mortality. Source of Support: Nil Conflict of Interest: None declared.