Pulmonary manifestations associated with positive anti neutrophil cytoplasmic antibodies: The tip of the iceberg.

Antibodies Antineutrophil cytoplasmic Histological techniques Lung diseases Tomography X-Ray Computed

Journal

Respiratory medicine case reports
ISSN: 2213-0071
Titre abrégé: Respir Med Case Rep
Pays: England
ID NLM: 101604463

Informations de publication

Date de publication:
2024
Historique:
received: 12 08 2024
revised: 07 09 2024
accepted: 14 09 2024
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 30 9 2024
Statut: epublish

Résumé

Even though anti-neutrophil cytoplasmic antibodies (ANCA) are frequently linked to ANCA associated vasculitis (AAV), it's important to understand that other illnesses, including lung diseases, can also manifest as ANCA positivity. Finding the incriminated pathology might be difficult. To report four ANCA-associated cases with a diagnosis problem. Four patients were recruited from the allergo-pneumology department of the Fattouma Bourguiba University Hospital of Monastir, Tunisia, over two years (2020-2022). Indirect immunofluorescence technique on neutrophil cells (Euroimmun, Germany) was used for ANCA screening with a positivity limit of 1/20. ANCA typing was carried out by a line-blot technique (Euroimmun, Germany). This case series reports four cases (age range: 41-67 years, sex ratio: 0.3) that presented with pulmonary manifestations associated with ANCA positivity. Two patients had perinuclear ANCA with anti-myeloperoxidase on typing, and two cases had cytoplasmic ANCA with one case of anti-leukocyte proteinase 3 on typing. Final diagnoses were pulmonary tuberculosis (case 1), systemic lupus erythematosus (case 2), bronchiolitis obliterans organizing pneumonia (case 3), and pulmonary aspergillosis with AAV (case 4). A panel of diagnoses may be evoked in front of positive ANCA, making the diagnosis difficult to determine and requiring multidisciplinary interactions, with imaging and histological investigations having a crucial role in guiding the final decision.

Sections du résumé

Background UNASSIGNED
Even though anti-neutrophil cytoplasmic antibodies (ANCA) are frequently linked to ANCA associated vasculitis (AAV), it's important to understand that other illnesses, including lung diseases, can also manifest as ANCA positivity. Finding the incriminated pathology might be difficult.
Aim UNASSIGNED
To report four ANCA-associated cases with a diagnosis problem.
Methods UNASSIGNED
Four patients were recruited from the allergo-pneumology department of the Fattouma Bourguiba University Hospital of Monastir, Tunisia, over two years (2020-2022). Indirect immunofluorescence technique on neutrophil cells (Euroimmun, Germany) was used for ANCA screening with a positivity limit of 1/20. ANCA typing was carried out by a line-blot technique (Euroimmun, Germany).
Results UNASSIGNED
This case series reports four cases (age range: 41-67 years, sex ratio: 0.3) that presented with pulmonary manifestations associated with ANCA positivity. Two patients had perinuclear ANCA with anti-myeloperoxidase on typing, and two cases had cytoplasmic ANCA with one case of anti-leukocyte proteinase 3 on typing. Final diagnoses were pulmonary tuberculosis (case 1), systemic lupus erythematosus (case 2), bronchiolitis obliterans organizing pneumonia (case 3), and pulmonary aspergillosis with AAV (case 4).
Conclusion UNASSIGNED
A panel of diagnoses may be evoked in front of positive ANCA, making the diagnosis difficult to determine and requiring multidisciplinary interactions, with imaging and histological investigations having a crucial role in guiding the final decision.

Identifiants

pubmed: 39345929
doi: 10.1016/j.rmcr.2024.102113
pii: S2213-0071(24)00136-9
pmc: PMC11439551
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

102113

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper."

Auteurs

Rania Kaddoussi (R)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Mourad Elghali (M)

Laboratory of Immunology, University Hospital FB, Monastir, Tunisia.

Jamel Saad (J)

Radiology Department, University Hospital FB, Monastir, Tunisia.

Imene Chaabane (I)

Internal Medicine Department, University Hospital FB, Monastir, Tunisia.

Saoussen Cheikhm'hamed (S)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Souhir Ksissa (S)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Lobna Loued (L)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Ahmed Ben Saad (A)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Wajih Ghribi (W)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Asma Ghourabi (A)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Sameh Joober (S)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Nabil Sakly (N)

Laboratory of Immunology, University Hospital FB, Monastir, Tunisia.

Naceur Rouetbi (N)

Pneumology Department, University Hospital FB, Monastir, Tunisia.

Melek Kechida (M)

Internal Medicine Department, University Hospital FB, Monastir, Tunisia.

Classifications MeSH