A 78-year-old woman was referred to our university hospital due to dry cough, fever, and weight loss. Laboratory revealed blood eosinophilia, high ESR, CRP and LDH. Rheumatologic markers were negative. Chest X-ray showed ground glass opacities in upper lobes. Uveitis developed in the left eye 1 week after admission. Thorax CT revealed ground glass opacities, reticular appearence in the upper lobes, enlarged axillary and mediastinal lymph nodes. Bronchoalveolar lavage CD4/CD8 was 2.1 and had 48% eosinophils. Histopathologic examination revealed eosinophilic infiltration and non-caseating epitheloid granulomas in the lung and mediastinal lymph nodes without vasculitis. Symptoms, blood eosinophilia and initial thorax CT findings improved after two months of methylprednisolone treatment. Chronic eosinophilic pneumonia is a rare disease characterized by systemic and pulmonary manifestations. It may be associated with other diseases.
Idiopathic chronic eosinophilic pneumonia (CEP) is a rare disease characterized by pulmonary manifestations, eosinophilia, peripheral opacities on chest X-ray with a prompt response to steroid treatment [1-6]. CEP may be associated with other diseases [7,8]. Association of CEP with sarcoidosis is very unusual [9,10].
We report the case of a patient with coexisting sarcoidoisis and chronic eosinophilic pneumonia along with review of the literature.
A 78-year-old woman was hospitalized in September 2013 for dry cough, fever, and, weight loss of 6 kg over the last 4 months. Personal history included hypertension of 15 years. She was a nonsmoker. The patient was cachectic with loss of skin turgor. Blood pressure was 180/100 mm Hg. Respiratory rate was 18/minute. Physical examination revealed fine crackles over the left bazal zone, enlarged cervical, axillary and inguinal lymph nodes. Oxygen saturation was 94% on room air.
Laboratory data on admission included eosinophilia (2760/mm3, 25.3%, WBC: 10.870/mm3), mild normocytic anemia, a high ESR (117 mm/h), a high CRP (62 mg/L) and a high LDH (670 IU/L) level. Chest X-ray revealed bilateral upper lobe ground glass opacities. Blood smear showed increased number of eosinophils (
In the first week of her admission redness and pain developed in the left eye. Opthalmologic consultation revealed anterior uveitis. Thorax CT disclosed ground glass opacities, reticular appearence with intertistial thickening in both upper lobes, axillary and mediastinal enlarged lymph nodes (
cells, asteroid and Schaumann bodies compatible with sarcoidosis (
Based on these findins, a diagnosis of sarcoidosis with coexisting chronic eosinophilic pneumonia was made. The patient was commenced on 36 mg methylprednisolone daily. Patient symptoms, hematological findings (eosinophil count decreased to 310/mm3, 3%), BAL eosinophilia (eosinophil ratio decreased to 8%) and CT findings promptly improved after two months of treatment (
Our patient had clinical, radiological and pathological features of sarcoidosis associated with chronic eosinophilic pneumonia. Causes for eosinophilia such as drugs and infections were ruled out in this case. There was no evidence of vasculitis in the biopsy specimes. Consequently, idiopathic chronic eosinophilic pneumonia in regard to symptoms (weight loss, fever), pulmonary manifestations, blood eosinophilia, radiologic findings, exclusion of other etiologies with prompt response to steroid treatment, was diagnosed. On the other hand, uveitis, high serum ACE, pathology of transbronchial and lymph node biopsy specimens were compatible with sarcoidosis.
Idiopathic CEP is a rare disease of unknown origin characterized by respiratory and systemic symptoms, alveolar or blood eosinophilia, peripheral infiltrates on chest imaging with prompt response to steroid treatment [1-6]. CEP may be associated with other diseases [7,8]. Two cases of sarcoidosis and CEP coexistence have been reported [9,10].
BAL eosinophilia was 48% in our patient. This may be a feature of sarcoidosis but the increases are usually less than 8% and develop only in 5% of the patients [11,12]. In a review of 140 sarcoidosis patients, 14% had peripheral eosinophilia without any increase in lung eosinophils [
In this case, chronic eosinophilic pneumonia overlapped with sarcoidosis. The patient had symptoms of both diseases. The predominant nature of systemic symptoms with a high blood and BAL eosinophilia indicated CEP while presence of uveitis, high serum ACE, and non-caseating granulomas in TBLB pointed out to sarcoidosis. Consequently, the final diagnosis was sarcoidosis with coexistent chronic eosinophilic pneumonia. Systemic symptoms, blood eosinophilia, radiologic manifestations and BAL eosinophilia had prompt response to steroid treatment.
Eosinophilic lung diseases may occur due to a wide spectrum of pulmonary, or systemic etiologies [12,14]. Coexistence of sarcoidosis and CEP is a diagnostic challenge for the clinician because this occurence is extremely rare. Predominance of systemic symptoms with high peripheral eosinophil count are the most significant clues for the presence of chronic eosinophilic pneumonia coexisting with sarcoidosis.