Respiratory Failure With Diaphragmatic Palsy: A Rare Complication of Relapsing Polychondritis

CHEST Journal ◽  
2012 ◽  
Vol 142 (4) ◽  
pp. 992A
Author(s):  
Sridhar Badireddi ◽  
Mohammad Siddiqui
2021 ◽  
pp. 00953-2020
Author(s):  
Syeda Nafisa ◽  
Ben Messer ◽  
Beatrice Downie ◽  
Patience Ehilawa ◽  
William Kinnear ◽  
...  

The diaphragm is the main inspiratory muscle, and diaphragmatic weakness can lead to respiratory failure. Diaphragmatic weakness or paralysis commonly presents in association with more generalised neuromuscular disorders. However, it can be caused by other pathologies, such as trauma, compression, infection and inflammation [1]. Isolated diaphragmatic palsy (DP) is well-described [2], but often missed in adults [3], especially in bilateral diaphragmatic palsy (BDP) where both domes of the diaphragm are elevated.


2017 ◽  
Vol 4 (2) ◽  
pp. 31
Author(s):  
Leonidas Grigorakos ◽  
Katerina Tzortzopoulou ◽  
Anastasia Alexopoulou ◽  
Eva Sotiriou ◽  
Dimitra Markopoulou ◽  
...  

Background: Differentiated diagnosis of meningoencephalitis in elderly patients, when an uncommon picture of respiratory infection leading to acute hypercapnic respiratory failure (AHRF) and without neurological signs is present, may raise serious difficulties.Case report: Two patients aged 72 (patient 1) and 75 (patient 2), without any medical history of respiratory problems, were hospitalized during spring with influenza symptoms. Within less than 24 hours from their admission, patients developed AHFR, which led to disturbances of arterial blood gases (ABGs). They were intubated and transferred, mechanically ventilated, to our intensive care unit (ICU). After normalization of ABGs, a weaning process followed. Weaning was unsuccessful, as unexpected neurological semiotics occurred. The imaging of neurological MRI revealed no special damage apart from microangiopathy. Further investigations through lumbar puncture with cerebrospinal fluid (CSF) testing revealed meningoencephalitis. Antiviral treatment was applied and the outcome was successful for both patients.Conclusion: Critical care medical personnel should be aware of the event of viral meningoencephalitis in elderly patients with AHRF. Especially in the middle of influenza endemic periods, the management of elderly patients may not be appropriate, thus resulting in serious delays for a proper treatment of disease. Laboratory screening of blood and urine, as well as other body fluids, can help detect and determine brain infection. Results from these tests can help exclude other diseases that mimic meningoencephalitis. In cases of patients who are hospitalized in the ICU due to AHRF and do not exhibit neurological abnormalities from the onset of illness, lumbar puncture and check of CSF should be a routine examination. Prophylactic vaccination of high-risk groups may be of crucial importance for preventing complications in patients who develop meningoencephalitis. However, once infected with this disease, the positive outcome is highly dependent on the immediate diagnosis and proper treatment of patients in the ICU.


2015 ◽  
Vol 68 (11-12) ◽  
pp. 429-432 ◽  
Author(s):  
Eda Kilic Coban ◽  
Sedat Gez ◽  
Batuhan Kara ◽  
Aysun Soysal

1997 ◽  
Vol 20 (1) ◽  
pp. 52-59 ◽  
Author(s):  
Akikazu Kanou ◽  
Tomohiro Akimoto ◽  
Shigeto Kobayashi ◽  
Michiyo Tomita ◽  
Naoto Tamura ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-3
Author(s):  
Benjamin Chaucer ◽  
Augustus Demanes ◽  
Abriella Stone ◽  
Venkat Kakollu

Background. Relapsing Polychondritis is a rare rheumatologic condition with multisystem involvement. Common presenting symptoms are auricular and nasal chondritis. Common complications include hearing loss and cardiac involvement. An extremely rare complication is neurological involvement. Case report. We present a case of relapsing polychondritis resulting in stroke and discuss the current literature on this condition. Conclusion. To our knowledge, only 6 previous documented cases of stroke secondary to relapsing polychondritis exist in the current literature. This case represents a rare but important complication of relapsing polychondritis.


2021 ◽  
Vol 3 (3) ◽  
pp. 01-05
Author(s):  
Ferreira de Vasconcelos ◽  
José Antonio Pinto ◽  
Heloisa dos Santos Sobreira Nunes ◽  
Gabriella Spinola Jahic ◽  
Andréia Natalia Azevedo ◽  
...  

Relapsing Polychondritis is a rare, multisystem autoimmune disease still of unknown origin, characterized by recurrent inflammation of the hyaline cartilages. The involvement of Laryngotracheal cartilages in polychondritis is one of the most serious known complications, observed in 50% of patientswith worse prognosis. Among the causesof death, laryngotracheal stenosis associated with pneumonia or severe respiratory failure stands out, and may be found in 10% to 50% of patients with the disorder. We describe a case of relapsing polychondritis in a female patient, with dyspnea as an initial manifestation, in which Grade III Cotton-Myer Laryngotracheal Stenosis was later confirmed. During the 10 years of investigation, clinical treatment stabilized the disease, but the respiratory distress persisted, which prompted the patient to be submittedto surgical correction of laryngotracheal stenosis.


2014 ◽  
Vol 59 (9) ◽  
pp. e140-e143 ◽  
Author(s):  
S. Badireddi ◽  
M. F. Siddiqui ◽  
N. J. Boddu

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