Chocolate-Colored Pseudochylothorax in a Woman with a History of Pleuropulmonary Tuberculosis.
Journal
The American journal of case reports
ISSN: 1941-5923
Titre abrégé: Am J Case Rep
Pays: United States
ID NLM: 101489566
Informations de publication
Date de publication:
15 Jun 2023
15 Jun 2023
Historique:
medline:
16
6
2023
pubmed:
15
6
2023
entrez:
15
6
2023
Statut:
epublish
Résumé
BACKGROUND Pseudochylothorax is a rare entity, with only a few hundred case reports worldwide. It presents as a pleural effusion rich in lipids, typically with a cloudy, milky appearance. The diagnosis is made based on the levels of cholesterol and triglycerides in the pleural fluid. CASE REPORT This is the case report of a 55-year-old woman with a history of pleuropulmonary tuberculosis that was treated in childhood, with a new infection and treatment in adulthood that evolved to a left pleural effusion. Thirteen years after completing her last treatment for tuberculosis, the patient developed general fatigue and dyspnea on exertion. Computed tomography of the chest confirmed the presence of a pleural collection in the same location as in adolescence, suggesting a chronic evolution with encystation. The patient underwent ultrasound-guided diagnostic thoracentesis. The collected liquid was thick, chocolate-colored, with the following biochemical characteristics: pH, 7.3; glucose, 37.9 mg/dL; LDL, 2059.8 IU/L; total protein, 8.8 mg/dL; triglycerides, 90 mg/dL; adenosine deaminase, 56 U/L; and cholesterol, 300 mg/dL. The effusion was characterized as a pseudochylothorax. The cell count showed 631 000 leukocytes/µL, with 87.9% polymorphonuclear cells. Owing to the patient's respiratory symptoms, an evacuatory thoracentesis was performed. After the procedure, the patient's symptoms improved. CONCLUSIONS Although pseudochylothorax is a rare condition, its possibility must always be kept in mind to avoid the hazards of misdiagnosis. In addition to the 'classic' milky and machine oil appearance, a chocolate-colored appearance should also serve as a clue to the diagnosis of pseudochylothorax.
Identifiants
pubmed: 37317516
pii: 939473
doi: 10.12659/AJCR.939473
pmc: PMC10278666
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e939473Références
J Bronchology Interv Pulmonol. 2019 Apr;26(2):e16-e17
pubmed: 30908394
Clin Chest Med. 2021 Dec;42(4):667-675
pubmed: 34774173
Intern Med. 2022 Dec 28;:
pubmed: 36575018
Eur Respir J. 1997 May;10(5):1157-62
pubmed: 9163662
J Thorac Dis. 2016 Aug;8(8):2093-101
pubmed: 27621864
Br J Surg. 1997 Jan;84(1):15-20
pubmed: 9043440
J Gen Fam Med. 2017 Mar 21;18(1):38-41
pubmed: 29263988
Respiration. 1991;58(5-6):294-300
pubmed: 1792420
Arch Bronconeumol. 2022 Feb;58(2):173
pubmed: 33994244
Indian J Chest Dis Allied Sci. ;58(1):59-61
pubmed: 28394099
Chest. 2009 Oct;136(4):1144-1147
pubmed: 19809057
Chest. 1985 Sep;88(3):426-8
pubmed: 4028854
Respirology. 2011 Feb;16(2):238-43
pubmed: 21073678
Clin Chest Med. 1985 Mar;6(1):163-71
pubmed: 3847300
Respir Med. 2019 Oct;157:7-13
pubmed: 31454675
Semin Respir Crit Care Med. 2010 Dec;31(6):743-50
pubmed: 21213206
Am J Med Sci. 2008 Jan;335(1):16-20
pubmed: 18195578
Mayo Clin Proc. 1980 Nov;55(11):700-4
pubmed: 7442324
Chest. 2008 Jun;133(6):1436-1441
pubmed: 18339791
Semin Respir Crit Care Med. 2001 Dec;22(6):617-26
pubmed: 16088705