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Acute fibrinous and organising pneumonia: a case report and review of the literature
Journal of Medical Case Reports volume 3, Article number: 74 (2009)
Organising pneumonia is a distinct histopathological entity characterized by intra-alveolar buds of granulation tissue, called Masson bodies, which mainly comprise of activated fibroblasts and loose connective tissue. This histopathologic pattern has been described in idiopathic cases, characterizing cryptogenic organising pneumonia as well as in the context of pulmonary infection, drug-induced pneumonitis and following lung transplantation. Although distinct as a clinical and pathological entity, community organising pneumonia may present with atypical clinical and pathological features, such as intra-alveolar fillings of fibrin balls and organising tissue that resembles acute respiratory distress syndrome or diffuse alveolar damage. The latter characteristics constitute a recently described anatomoclinical entity called acute fibrinous and organising pneumonia.
Here, we describe a rare case of acute fibrinous and organising pneumonia, in an otherwise healthy 65-year-old Greek woman who complained of dry cough, fever, weight loss and progressive dyspnoea. She had never been a smoker. Her clinical symptoms showed a rapid deterioration in the two weeks before admission, despite a course of oral antibiotics. After excluding infection and malignancy with routine laboratory tests and flexible bronchoscopy, high resolution computed tomography and video assisted thoracoscopic lung biopsy were performed. Diagnosis was based on radiological features typical of community organising pneumonia coupled with pathologic features characteristic of acute fibrinous and organising pneumonia. The patient was treated with corticosteroids and showed excellent clinical and radiological response three months after treatment initiation.
Acute fibrinous and organising pneumonia is an extremely rare pathologic entity, often misdiagnosed as typical community organising pneumonia. To our knowledge, this is the seventh case of acute fibrinous and organising pneumonia in the literature, with no identifiable cause or association in a female patient, with no underlying lung disease or known exposures and with an unremarkable previous medical history. We highlight the need for careful review of lung biopsies from patients with clinical and radiologic characteristics typical of community organising pneumonia. Although it remains uncertain whether fibrin alters the favourable prognosis and treatment response of community organising pneumonia, it becomes obvious that a thorough pathologic review, apart from establishing the diagnosis of acute fibrinous and organising pneumonia, may predict a more unfavorable outcome therefore alerting the clinician to administer more aggressive and prolonged therapeutic regimens.
The pathological pattern of organising pneumonia associated with intra-alveolar fibrin deposition has been individualised by Beasley et al in 2002  as acute fibrinous and organising pneumonia (AFOP). It was positioned as an under recognized variant of diffuse alveolar damage (DAD), cryptogenic organising pneumonia (COP) and eosinophilic pneumonia (EP). AFOP is an extremely rare, yet not fully accepted as a distinct anatomoclinical, entity that may occur in an idiopathic context or in association with a wide spectrum of clinical conditions, including collagen vascular diseases, adverse drug reactions, occupational or environmental exposures, as well as various infections. AFOP has been reported to present with two clinical profiles of progression, both of them having similar incidences: a fulminant illness often overlapping with acute respiratory distress syndrome (ARDS) and a more subacute clinical profile, with excellent treatment response and prognosis , similar to that seen in COP . The radiographic findings of AFOP are almost identical to those seen in COP, consistent with multiple, migratory, patchy, diffuse, alveolar opacities with peripheral and bilateral distribution [1–5]. We have observed crescentic and ring-shaped opacities in COP cases (4), multiple cavitary lesions with hemoptysis , and fatal pneumothorax .
In this manuscript, we report the seventh case of idiopathic AFOP in a female patient, with no underlying lung disease or known exposures and with an unremarkable previous medical history. The patient presented with a more subacute and mild clinical profile consisting of fever, weight loss and progressive dyspnoea and showed an excellent clinical and radiological response following corticosteroid administration.
A 65-year-old Greek woman was admitted to the outpatient clinic of our hospital due to dry cough, fever, weight loss of 5 kg and progressive breathlessness for one month. Her clinical symptoms showed a rapid deterioration during the last two weeks before admission, despite a course of oral antibiotics (macrolide and b-lactam). She was a lifetime non-smoker and used to work in an environment with no known exposures to chemicals, fumes, dust and other environmental or occupational allergens. Her previous medical history included osteoporosis and hyperlipidemia, both of them under appropriate medical treatment.
On physical examination she was in extremis, had tachypnea (respiratory rate 20/min), and tachycardia (heart rate 100 bpm). She had no hypoxaemia (partial pressure of oxygen 84 mmHg) on arterial blood gas analysis. She had no clubbing, skin lesions, cervical lymphadenopathy or joint swelling. Auscultation of the lungs revealed crepitations with diminished breath sounds over the lower right hemithorax, while inspiratory crackles in the posterior left chest were also noticed. Cardiovascular, abdominal and neurological system examinations were unremarkable. The erythrocyte sedimentation rate was 65 mm.h-1. The rest of the physical examination and routine laboratory tests, including white blood cell count and differential, red blood cell count, liver and renal function, and serum C-reactive protein, were normal. Laboratory tests for collagen vascular disease and vasculitis, including ANA, ENA and ANCA antibodies, were also negative. Pulmonary function test parameters were within normal range excluding a slight decrease (60% of predicted value) in carbon monoxide diffusing capacity (DLCO). Chest radiograph (Figure 1) followed by high resolution computed tomography (HRCT) of the lung were then performed and showed patchy areas of consolidation with a predominantly peripheral and subpleural distribution mainly in the right lung (Figure 2). The tuberculin skin test was negative. Flexible bronchoscopy followed by bronchoalveolar lavage (BAL) was undertaken and revealed no endobrochial lesion. Bronchial lavage fluid specimens were smear and culture negative for common bacteria and acid-bacilli. In addition, BAL differential cell count revealed a mild lymphocytosis (16%) with a normal CD4/CD8 T cells ratio. In order to exclude malignancy, video-assisted thoracoscopic lung biopsy from multiple lesions of the right lower lobe was undertaken a week after presentation. Extensive pathologic review of lung specimens revealed preservation of the lung architecture with patchy distribution of intra-alveolar fibrin, in the form of fibrin "balls" (Figure 3, insert a), associated with organising pneumonia, consisting of intraluminal loose connective tissue within the alveolar ducts and bronchioles (Figure 3, insert b). The latter observations were consistent with the diagnosis of a rare clinico-pathological entity called AFOP.
High doses of oral corticosteroid (1 mg/kg of weight) as a monotherapy were then commenced with dramatic symptomatic improvement after 48 hours and near-complete resolution of radiograph infiltrates by the 7th day of treatment. However, she showed poor compliance and discontinued corticosteroid treatment due to prominent side effects including tremor, cushinoid face, growth of facial hair, cataract development in both eyes, mood changes and insomnia. She then presented with relapsing clinical symptoms including fever, progressive dyspnoea and dry cough. HRCT was then undertaken (Figure 4) and demonstrated deterioration of the disease with extensive subpleural and peribronchovascular consolidation in the right upper lobe. She was restarted on oral corticosteroids resulting in rapid clinical and radiological improvement. She remained well and her HRCT (Figure 5) was significantly improved after three months of continuous corticosteroid therapy. The patient is now on a tapering dose.
To the best of our knowledge, this is the seventh case of AFOP in the literature, with no identifiable cause or association in a female patient, with no underlying lung disease or known exposures and with previous medical history almost unremarkable. AFOP is an extremely rare pathologic entity, first described by Beasley et al . While the histologic hallmark of COP is intra-alveolar buds of granulation tissue that share similarities with the fibroblastic foci of usual interstitial pneumonia (UIP) , AFOP is also characterized by prominent intra-alveolar fibrin deposition (fibrin balls) resulting in a morphological pattern that may represent an underreported variant of DAD, COP and EP [1–3]. It has been reported that AFOP may occur in an idiopathic context or in association with a wide spectrum of clinical conditions, including collagen vascular diseases, adverse drug reactions, occupational or environmental exposures, as well as various infections. Furthermore, several cases have no identifiable origin or association and consequently are named idiopathic [1–3]. In addition, a case of AFOP in a patient with chronic renal failure being on hemodialysis has also been reported .
Retrospective follow-up of these patients revealed two clinical profiles of disease progression, both of them presented with similar incidence: a fulminant illness often overlapping with ARDS, both clinically and pathologically, and a more subacute illness, with favorable treatment response and disease progressiveness . The latter seems to resemble COP in terms of prognosis and recovery following corticosteroid treatment. However, the presence of fibrin in the organising lesions has been associated with less favorable treatment response [2, 8]. The radiographic findings of AFOP are almost identical to those seen in COP, consistent with multiple, migratory, patchy, diffuse, alveolar opacities with peripheral and bilateral distribution. In our case, HRCT revealed subpleural and peribronchovascular band-like consolidations with air-bronchograms and no predominant lobe distribution, imaging features typical of COP. However, in addition to that, some of the band-like consolidations formed a peripheral circle engulfing a ground-glass centre, resembling one of the more atypical faces of COP: the "reversed halo sign". HRCT findings of AFOP have been described only in one other case report presenting with a solitary nodule with an air-bronchogram , which is also included in the more atypical and rare HRCT appearances of classic COP.
In our case, the clinical presentation of the patient, the almost complete treatment response and the clinical and the radiographic relapse following corticosteroid discontinuation, were typical of COP. There was no evidence of infection, malignancy or any other factors known to be related with organising pneumonia, such as collagen vascular diseases, drug-induced interstitial lung disease or allergic reactions. However, lung biopsy extensively reviewed by an expert pathologist, verified a rather unexpected histologic pattern. Based on the aforementioned data and the mild clinical course of the patient we can conclude that our patient suffered from a more subacute version of the disease. Nevertheless, it is important to stress that the latter seems to be under-diagnosed or misinterpreted as typical COP, as has been demonstrated by recent reports [9, 10]. Therefore, we highlight the need of careful reviewing lung biopsies from patients with clinical and radiological characteristics typical of COP. Although, it remains uncertain whether fibrin alters the favourable prognosis and treatment response of COP, it becomes obvious that a thorough pathologic review, apart from establishing the diagnosis of AFOP, may predict a more unfavourable outcome, therefore compelling the clinician to administer more aggressive and prolonged therapeutic regimens.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
cryptogenic organising pneumonia
acute fibrinous and organising pneumonia
diffuse alveolar damage
acute respiratory distress syndrome
- DLCO :
carbon monoxide diffusing capacity
high resolution computed tomography
usual interstitial pneumonia
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The authors declare that they have no competing interests.
AT performed the physical examination of the patient, analysed clinical and laboratory findings and was a major contributor in writing the manuscript. AK performed the pathologic review of lung specimens, and was a major contributor in writing the manuscript. AO undertook the HRCT and analysed the radiological findings of the disease. MF and PS performed the bronchoscopy and BAL analysis. DM performed the video-assisted thoracoscopic lung biopsy. PZ performed the pulmonary function tests and examined the patient on resubmission. DB and AA analyzed the manuscript for any important intellectual content. All authors read and approved the final manuscript.
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Tzouvelekis, A., Koutsopoulos, A., Oikonomou, A. et al. Acute fibrinous and organising pneumonia: a case report and review of the literature. J Med Case Reports 3, 74 (2009). https://doi.org/10.1186/1752-1947-3-74
- High Resolution Compute Tomography
- Diffuse Alveolar Damage
- Eosinophilic Pneumonia
- Cryptogenic Organise Pneumonia
- Underlie Lung Disease