Interstitial lung diseases are very heterogeneous. We present a case of usual interstitial pneumonia pattern on high resolution computed tomography of the chest that was diagnosed successfully after multi-disciplinary discussion. Pulmonologists should be aware of the pitfalls in the diagnostic management of interstitial lung diseases, especially in cases with atypical clinical presentation and systemic signs and symptoms

Afthinos, Andreas

Papanikolaou, Ilias C

Papoudou-Bai, Alexandra

Repousis, Panagiotis

English

Via Medica Journals

PRACA ORYGINALNA274LETTER T  THE EDITORwww.journals.viamedica.plAddress for correspondence: Ilias Papanikolaou, Pulmonary Department, Corfu General Hospital, Corfu Greece; e-mail: icpapanikolaou@hotmail.comDOI: 10.5603/ARM.2019.0069Received: 24.10.2019Copyright © 2019 PTChPISSN 2451–4934Ilias C. Papanikolaou1, Andreas Afthinos1, Alexandra Papoudou-Bai2, Panagiotis Repousis31Pulmonary Department, Corfu General Hospital, Corfu, Greece2Pathology Unit, Ioannina University Hospital, Ioannina, Greece3Hematology Department, Metaxa Hospital, Athens, GreeceIntegrating multi-disciplinary discussion in clinical practiceCase presentationA 68 year-old male was referred to our cli-nic in order to investigate an abnormal chest radiography that was performed during work-up of an anemia with unknown onset. The patient reported shortness of breath over the last 4 months (MMRC scale 2), dry cough, fatigue and an irregular fever up to 38°C two times/week. He is a former smoker (80 pack years) with no prior illnesses and without environmental or occupational hazards.On physical examination, the patient had conjunctival paleness, diffuse crackles on au-scultation of the lower lung fields bilaterally and palpable inguinal lymph nodes. Pulmonary function testing showed a mixed obstructive-re-strictive defect and a moderately compromised diffusing capacity (FEV1 72%, FVC 81%, FEV1/ /FVC 0.74, TLC 71%, DLCO 52%). Blood tests showed hematocrit 37%, hemoglobin 12.3 g/dL, an erythrocyte sedimentation rate of 40 mm, and a C-reactive protein value of 6 mg/dL. An auto-immunity panel was normal. A High-Resolution Computed Tomography (HRCT) scan showed a probable usual interstitial pneumonia (UIP) pattern with subpleural distribution consisting of reticulation and traction bronchiectasis, minimal ground-glass opacities, para-septal emphysema and one middle lobe nodule (Figure 1). A posi-tron emission tomography (PET)-CT scan was performed to evaluate the nodule and to inve-stigate enlarged lymph nodes in the abdomen. It demonstrated uptake in bones (spine, ribs, sca-pula), mediastinum, a pulmonary nodule, liver, spleen, iliac and inguinal lymph nodes (Figure 1). Bronchoalveolar lavage was then performed and it showed increased cellularity (28 × 106 cells) with lymphocyte predominance (neutrophils 5%, lymphocytes 27%, eosinophils 1%, macrophages 67%). Perls’ and CD1a stains were negative.Multi-disciplinary discussion (MDD) con-sisted of consultation between a radiologist, a pulmonologist, a pathologist and a hematologist. Together, they recognized a case of probable UIP with a non-diagnostic BAL demonstrating lym-Figure 1. A. High resolution computed tomography scan of the lun-gs showing subpleural lower lobes reticulation, ground-glass opa-cities and bronciolectasis; B. Reticulation and a middle lobe nodule; C. Positron emission tomography-computed tomography scan sho-wing pulmonary nodule and lymph nodes uptake as well as D. diffuse uptake in skeleton, spleen and lymph nodesA BC DIlias C. Papanikolaou et al., Integrating multi-disciplinary discussion in clinical practice275www.journals.viamedica.plphocytosis in a clinical context not typical for idiopathic pulmonary fibrosis (IPF). In addition, there were many systemic symptoms and findings suggestive of possible alternative diagnoses. Histological diagnosis was deemed necessary; a decision was made to pursue a surgical biopsy from the most easily assessible site. Inguinal lymph node pathology demonstrated numerous Langerhans cells with characteristic grooved nuclei which stained immunohistochemically positive for langerin and CD1a (Figure 2). MDD considered the findings and a diagnosis of mul-tisystemic Langerhans cell histiocytosis (LCH) was established.DiscussionOur patient’s HRCT pattern was classified as having a probable UIP pattern (reticulation, subpleural distribution, without honeycombing) based on the latest ATS/ERS/JRS/ALAT guidelines for the diagnosis of IPF [1]. Although Langerhans cell histiocytosis is considered among the etio-logies of the alternative diagnosis HRCT pattern, this patient’s scan had no cysts, no profound ground-glass opacities and only one nodule. The probable UIP pattern, however, needs to be inve-stigated further. The same guidelines provide con-ditional recommendation for an MDD procedure in order to select further diagnostic procedures in the case of a probable UIP pattern, indicating BAL cellular analysis and surgical lung biopsy as potential next steps.Fleishner’s society white paper on IPF diagnostic criteria identifies the presence of systemic features (like in this case) as a key checklist component for a diagnosis alternative to IPF [2]. Moreover, the authors conclude that MDD is necessary when the clinical context or the HRCT pattern is/are indeterminate for IPF. The clinical context in the case we present was clearly indeterminate considering the systemic features and multi-organ involvement. Accor-ding to the authors, the outcome of the MDD will lead to a decision on whether to perform additional investigations, BAL or surgical lung biopsy and to integrate, after a biopsy is per-formed, the clinical, imaging and pathological features. Based on these conclusions, MDD may provide guidance as to what is the most suitable procedure.  A clinical practice guideline by the American Thoracic Society recommends performing BAL in patients that lack a confident UIP pattern on HRCT and who can tolerate the procedure [3]. BAL may be diagnostic in rare diseases and may narrow the differential diagnosis by the respective cellular profile (lymphocytic, neutrophilic or eo-sinophilic). In our case, BAL was CD1a negative and demonstrated lymphocytosis. Therefore, the need for a surgical diagnosis was not obviated. BAL may precede surgical lung biopsy as a less interventional procedure when the differential diagnosis includes rare diseases or diseases with a predominant lymphocytic or eosinophilic cel-lular profile as an adjunct to diagnosis. Langerhans cell histiocytosis (LCH), as clas-sified by the World Health Organization, is a rare dendritic cell disorder [4]. Acute disseminated multisystem disease is commonly seen in child-ren less than three years old [5]. Our patient was started on prednisolone plus vinblastine, with partial response. Of note, the pulmonary nodule completely disappeared after the initial regimen and did not re-appear. The prognosis was poor and our patient passed away 13 months after initial diagnosis. In the era of modern anti-fibrotic medica-tions approved for use in IPF, we present a case of probable UIP other than IPF. We would like to point out that the pulmonologist should always rigorously investigate extra-pulmonary signs and symptoms when present, and not restrict his differential diagnosis to solely lung-oriented diffuse pulmonary diseases. Provisional IPF dia-gnosis that allows to avoid invasive procedures like surgical lung biopsy is useful but only when used in the appropriate clinical setting.   Figure 2. A. Lymph node involved in Langerhans cell histiocytosis exhibited partial effacement of normal nodal architecture (H&E, magni-ficationX40); B. Lymph node biopsy showed the presence of numerous Langerhans cells with the characteristic grooved nuclei (H&E, magni-ficationX400), (inset: magnificationX600). No nuclear atypia, necrosis or increased number of mitotic figures were noted; C. Langerhans cells stained immunohistochemically positive for CD1a and D. langerin (CD207) (DAB, magnificationX100)AC DBAdvances in Respiratory Medicine 2019, vol. 87, no. 3, pages 274–276 276 www.journals.viamedica.plConflict of interestNone declared.References:1. Raghu G, Remy-Jardin M, Myers JL, et al. Diagnosis of idiopathic pulmonary fibrosis: an official ATS/ERS/JRS/ALAT clinical practice guideline. Am J Respir Crit Care Med. 2018; 198(5): e44–e68, doi: 10.1164/rccm.201807-1255ST., indexed in Pubmed: 30168753.2. Lynch DA, Sverzellati N, Travis WD, et al. Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper. Lancet Respir Med. 2018; 6(2): 138–153, doi: 10.1016/S2213-2600(17)30433-2, indexed in Pubmed: 29154106.3. Meyer KC, Raghu G, Baughman RP, et al. An official American Thoracic Society clinical practice guideline: the clinical uti-lity of bronchoalveolar lavage cellular analysis in interstitial lung disease. Am J Respir Crit Care Med. 2012; 185(9): 1004–1014, doi: 10.1164/rccm.201202-0320ST, indexed in Pubmed: 22550210.4. Jaffe R, Weiss LM, Facchetti F, et al. Tumours derived from Langerhans cells. World Health Organization Classification of Tumours of Haematooietic and Lymhoid Tissues. Swer-dlow SH, Camo E, Harris NL (ed). IARC Press, Lyon 2008: 358.5. DeMartino E, Go RS, Vassallo R. Langerhans cell histiocytosis and other histiocytic diseases of the lung. Clin Chest Med. 2016; 37(3): 421–430, doi: 10.1016/j.ccm.2016.04.005, indexed in Pubmed: 27514589.\

Integrating multi-disciplinary discussion in clinical practice

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Integrating multi-disciplinary discussion in clinical practice

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