Special Issue "Diagnosis and Management of Sarcoidosis—A Multifaced Disease"

A special issue of Diagnostics (ISSN 2075-4418). This special issue belongs to the section "Pathology and Molecular Diagnostics".

Deadline for manuscript submissions: 31 December 2023 | Viewed by 738

Special Issue Editors

First Department of Lung Diseases, National Tuberculosis and Lung Diseases Research Institute, 01-138 Warsaw, Poland
Interests: cardiac sarcoidosis; venous thromboembolism management and treatment; interstitial lung diseases, diagnosis and treatment; COVID-19 lung disease; pericardial diseases
Special Issues, Collections and Topics in MDPI journals
National Institute of Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland
Interests: cardiac sarcoidosis; venous thromboembolism management and treatment; interstitial lung diseases, diagnosis and treatment; COVID-19 lung disease; pericardial diseases

Special Issue Information

Dear Colleagues,

Sarcoidosis is a systemic granulomatous disease of unknown origin, involving many organs. One of the pathogenic concepts is an aberrant immune response to an unknown inducer, possibly of bacterial origin.

The most frequent localisation of the disease is the lymphatic system of the lungs. Although in the majority of patients, the spontaneous regression of lung disease is observed; occasionally, lung fibrosis develops. The debate concerning the predictors of such an unfavourable course is still ongoing.

The most dramatic clinical scenario concern cardiac sarcoidosis, which may cause sudden cardiac death due to rhythm and/or conduction disturbances. The diagnostic algorithm of cardiac sarcoidosis is evolving, with MRI, PET-CT and PET-MRI imaging applied.

The other life-threatening complication of sarcoidosis is hypercalcaemia combined with acute renal insufficiency. The growing frequency of such a complication is caused by the increased use of vitamin D and calcium as dietary supplements.

The ERS sarcoidosis guidelines issued in 2021, recommend prompt treatment with corticosteroids in the case of life-threatening complications such as cardiac sarcoidosis or neurosarcoidosis. Another indication of life-saving therapy, not covered by ERS guidelines, is sarcoidosis-related hypercalcaemia. The rationale for prompt therapy in the remaining patients is less clear.

Having this in mind we invite the Authors to contribute with research articles, reviews of the literature, imaging studies and case presentations to the present Special Issue entitled: “Diagnosis and Management of Sarcoidosis—a Multifaced Disease.”

The present Special Issue will concern most actual problems:

  1. Diagnosis and treatment of cardiac sarcoidosis;
  2. Pericardial effusion in the course of sarcoidosis—management and treatment;
  3. Mechanisms of hypercalcemia in sarcoidosis and their prevention;
  4. Role of bacterial antigens in the pathogenesis of sarcoidosis;
  5. Predictors of lung fibrosis in sarcoidosis;
  6. Links between sarcoidosis and neoplastic disease;
  7. Sarcoidosis is a risk factor for venous thromboembolism.

We hope that the published data will contribute to scientific discussion concerning diagnosis and treatment of this multifaced disease.

Prof. Dr. Monika Szturmowicz
Prof. Dr. Witold Z. Tomkowski
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Diagnostics is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • sarcoidosis
  • interstitial lung disease
  • lung fibrosis
  • diagnosis
  • imaging
  • cardiac sarcoidosis
  • nuclear magnetic resonance
  • PET CT
  • pulmonary embolism
  • pulmonary hypertension
  • neurosarcoidosis
  • vision disturbances
  • bone sarcoidosis
  • hypercalcaemia
  • renal insufficiency
  • vitamin D metabolism
  • pathogenesis
  • IGRA
  • treatment

Published Papers (1 paper)

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Case Report
Sudden Vision Loss Due to Optic Neuritis—An Uncommon Presentation of Neurosarcoidosis
Diagnostics 2023, 13(15), 2579; https://doi.org/10.3390/diagnostics13152579 - 03 Aug 2023
Viewed by 497
Abstract
Sarcoidosis is a systemic, granulomatous disease of unknown etiology, most often manifested by mediastinal and hilar lymph node enlargement and parenchymal nodules in the lungs. However, it may involve any other organ. Neuro-sarcoidosis, a condition that affects up to 20% of sarcoidosis patients, [...] Read more.
Sarcoidosis is a systemic, granulomatous disease of unknown etiology, most often manifested by mediastinal and hilar lymph node enlargement and parenchymal nodules in the lungs. However, it may involve any other organ. Neuro-sarcoidosis, a condition that affects up to 20% of sarcoidosis patients, can be found in any part of the central or peripheral nervous system and has important ophthalmic and neuro-ophthalmic manifestations. We present two patients with sudden vision loss due to neurosarcoidosis. In both cases, biopsy of the mediastinal lymph node showed non-caseating granulomas consistent with sarcoidosis. Treatment involved high doses of methylprednisolone intravenously, followed by topical dexamethasone eye drops in the first case and a systemic steroid treatment in the second, resulting in symptom relief. Those two cases demonstrate that sarcoidosis should be considered as a differential diagnosis in cases of optic neuritis. Full article
(This article belongs to the Special Issue Diagnosis and Management of Sarcoidosis—A Multifaced Disease)
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