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1.
The Korean Journal of Critical Care Medicine ; : 162-168, 2016.
Artigo em Inglês | WPRIM | ID: wpr-770929

RESUMO

Pnuemocystis jirovecii pneumonia (PJP) is one of leading causes of acute respiratory failure in patients infected with human immunodeficiency virus (HIV), and the mortality rate remains high in mechanically ventilated HIV patients with PJP. There are several reported cases who received extracorporeal membrane oxygenation (ECMO) treatment for respiratory failure associated with severe PJP in HIV-infected patients. We report a patient who was newly diagnosed with HIV and PJP whose condition worsened after highly active antiretroviral therapy (HAART) initiation and progressed to acute respiratory distress syndrome requiring veno-venous ECMO. The patient recovered from PJP and is undergoing treatment with HAART. ECMO support can be an effective life-saving salvage therapy for acute respiratory failure refractory to mechanical ventilation following HAART in HIV-infected patients with severe PJP.


Assuntos
Humanos , Terapia Antirretroviral de Alta Atividade , Oxigenação por Membrana Extracorpórea , HIV , Mortalidade , Pneumocystis carinii , Pneumocystis , Pneumonia , Respiração Artificial , Síndrome do Desconforto Respiratório , Insuficiência Respiratória , Terapia de Salvação
2.
Korean Journal of Critical Care Medicine ; : 162-168, 2016.
Artigo em Inglês | WPRIM | ID: wpr-42553

RESUMO

Pnuemocystis jirovecii pneumonia (PJP) is one of leading causes of acute respiratory failure in patients infected with human immunodeficiency virus (HIV), and the mortality rate remains high in mechanically ventilated HIV patients with PJP. There are several reported cases who received extracorporeal membrane oxygenation (ECMO) treatment for respiratory failure associated with severe PJP in HIV-infected patients. We report a patient who was newly diagnosed with HIV and PJP whose condition worsened after highly active antiretroviral therapy (HAART) initiation and progressed to acute respiratory distress syndrome requiring veno-venous ECMO. The patient recovered from PJP and is undergoing treatment with HAART. ECMO support can be an effective life-saving salvage therapy for acute respiratory failure refractory to mechanical ventilation following HAART in HIV-infected patients with severe PJP.


Assuntos
Humanos , Terapia Antirretroviral de Alta Atividade , Oxigenação por Membrana Extracorpórea , HIV , Mortalidade , Pneumocystis carinii , Pneumocystis , Pneumonia , Respiração Artificial , Síndrome do Desconforto Respiratório , Insuficiência Respiratória , Terapia de Salvação
3.
The Korean Journal of Critical Care Medicine ; : 212-217, 2015.
Artigo em Inglês | WPRIM | ID: wpr-770877

RESUMO

In connective tissue diseases, autoantibodies cause pulmonary interstitial inflammation and fibrosis, and patients require treatment with an immunosuppressive agent such as a steroid. Dermatomyositis is an incurable, uncommon form of connective tissue disease that occasionally causes diffuse pulmonary inflammation leading to acute severe respiratory failure. In such cases, the prognosis is very poor despite treatment with high-dose steroid. In the present case, a 46-year-old man was admitted to our hospital with dyspnea. He was diagnosed with dermatomyositis combined with cryptogenic organizing pneumonia (COP) with respiratory failure and underwent treatment with steroid and an immunosuppressive agent, but the COP was not improved. However, the respiratory failure did improve after treatment with intravenous immunoglobulin, which therefore can be considered a treatment option in cases where steroids and immunosuppressive agents are ineffective.


Assuntos
Humanos , Pessoa de Meia-Idade , Autoanticorpos , Doenças do Tecido Conjuntivo , Pneumonia em Organização Criptogênica , Dermatomiosite , Dispneia , Fibrose , Imunoglobulinas , Imunossupressores , Inflamação , Doenças Pulmonares Intersticiais , Pneumonia , Prognóstico , Insuficiência Respiratória , Esteroides
4.
Journal of the Korean Geriatrics Society ; : 248-253, 2015.
Artigo em Coreano | WPRIM | ID: wpr-39491

RESUMO

A pleurobiliary fistula is an abnormal communication between the biliary system and the pleural space. It has rarely been reported after percutaneous transhepatic gallbladder drainage (PTGBD). Here, we report the case of an 88-year-old man with bilious pleural infection via pleurobiliary fistula following PTGBD. The patient had a fever, dyspnea and right pleuritic chest pain. The PTGBD was performed 2 months prior to treat acute cholecystitis with large gallstones. Chest radiography demonstrated a right pleural effusion and a computed tomography of the abdomen showed a pleurobiliary fistula tract associated with the previous PTGBD. A drainage tube was inserted into the right pleural effusion, and the bilious pleural fluid infected with Escherichia coli was drained. Careful approach to PTGBD procedure and reducing duration of catheter placement should prevent fistula formation. As a rare complication of PTGBD, practitioners should be aware of the potential of pleural infection by a pleurobiliary fistula tract.


Assuntos
Idoso de 80 Anos ou mais , Humanos , Abdome , Fístula Biliar , Sistema Biliar , Catéteres , Dor no Peito , Colecistite Aguda , Drenagem , Dispneia , Escherichia coli , Febre , Fístula , Vesícula Biliar , Cálculos Biliares , Derrame Pleural , Radiografia , Tórax
5.
Korean Journal of Critical Care Medicine ; : 212-217, 2015.
Artigo em Inglês | WPRIM | ID: wpr-33301

RESUMO

In connective tissue diseases, autoantibodies cause pulmonary interstitial inflammation and fibrosis, and patients require treatment with an immunosuppressive agent such as a steroid. Dermatomyositis is an incurable, uncommon form of connective tissue disease that occasionally causes diffuse pulmonary inflammation leading to acute severe respiratory failure. In such cases, the prognosis is very poor despite treatment with high-dose steroid. In the present case, a 46-year-old man was admitted to our hospital with dyspnea. He was diagnosed with dermatomyositis combined with cryptogenic organizing pneumonia (COP) with respiratory failure and underwent treatment with steroid and an immunosuppressive agent, but the COP was not improved. However, the respiratory failure did improve after treatment with intravenous immunoglobulin, which therefore can be considered a treatment option in cases where steroids and immunosuppressive agents are ineffective.


Assuntos
Humanos , Pessoa de Meia-Idade , Autoanticorpos , Doenças do Tecido Conjuntivo , Pneumonia em Organização Criptogênica , Dermatomiosite , Dispneia , Fibrose , Imunoglobulinas , Imunossupressores , Inflamação , Doenças Pulmonares Intersticiais , Pneumonia , Prognóstico , Insuficiência Respiratória , Esteroides
6.
Tuberculosis and Respiratory Diseases ; : 445-449, 2015.
Artigo em Inglês | WPRIM | ID: wpr-149063

RESUMO

Occupational lung diseases are caused by several toxic substances including heavy metals; however, the exact pathologic mechanisms remain unknown. In the workplace, dental technicians are often exposed to heavy metals such as cobalt, nickel, or beryllium and occasionally develop occupational lung diseases. We described a case of occupational lung disease in a patient who was employed as a dental technician for over a decade. A 31-year-old, non-smoking woman presented with productive cough and shortness of breath of several weeks duration. Chest computed tomography revealed a large number of scattered, bilateral small pulmonary nodules throughout the lung field, and multiple mediastinal lymph nodes enlargement. Percutaneous needle biopsy showed multifocal small granulomas with foreign body type giant cells suggestive of heavy metals inhalation. The patient's condition improved on simple avoidance strategy for several months. This case highlighted the importance of proper workplace safety.


Assuntos
Adulto , Feminino , Humanos , Berílio , Biópsia por Agulha , Cobalto , Tosse , Técnicos em Prótese Dentária , Dispneia , Corpos Estranhos , Células Gigantes de Corpo Estranho , Granuloma , Inalação , Pulmão , Pneumopatias , Linfonodos , Metais Pesados , Níquel , Tórax
7.
Tuberculosis and Respiratory Diseases ; : 141-144, 2014.
Artigo em Inglês | WPRIM | ID: wpr-103197

RESUMO

Invasive pulmonary aspergillosis (IPA) is rarely reported in patients who have normal immune function. Recently, IPA risk was reported in nonimmunocompromised hosts, such as patients with chronic obstructive pulmonary disease and critically ill patients in intensive care units. Moreover, influenza infection is also believed to be associated with IPA among immunocompetent patients. However, most reports on IPA with influenza A infection, including pandemic influenza H1N1, and IPA associated with influenza B infection were scarcely reported. Here, we report probable IPA with a fatal clinical course in an immunocompetent patient with influenza B infection. We demonstrate IPA as a possible complication in immunocompetent patients with influenza B infection. Early clinical suspicion of IPA and timely antifungal therapy are required for better outcomes in such cases.


Assuntos
Humanos , Estado Terminal , Imunocompetência , Vírus da Influenza B , Influenza Humana , Unidades de Terapia Intensiva , Aspergilose Pulmonar Invasiva , Pandemias , Doença Pulmonar Obstrutiva Crônica
8.
The Korean Journal of Critical Care Medicine ; : 336-339, 2013.
Artigo em Coreano | WPRIM | ID: wpr-646915

RESUMO

In Asia, snakebites are estimated to affect 4 million people every year, and of these, 100,000 people are estimated to die. In Korea, snakebites occur frequently from the spring to the fall, but their importance is often overlooked. Fatal complications, including acute respiratory distress and acute kidney injury, can occur, and in some cases, severe hemorrhage results from coagulopathy. There have been only a few cases of snakebite-induced liver or intestinal bleeding, but to our knowledge, spontaneous bleeding from the spleen has not been previously reported. Here, we report the case of a 61-year-old male who visited the emergency room with abrupt abdominal pain due to hemoperitoneum associated with splenic hemorrhage after a snakebite.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Dor Abdominal , Injúria Renal Aguda , Ásia , Emergências , Hemoperitônio , Hemorragia , Coreia (Geográfico) , Fígado , Mordeduras de Serpentes , Baço
9.
The Journal of the Korean Society for Transplantation ; : 132-137, 2013.
Artigo em Coreano | WPRIM | ID: wpr-29957

RESUMO

Cryptococcosis commonly affects patients with immune dysfunction, as in the case of immunosuppression in organ transplant patients or as acquired immunodeficiency syndrome in patients afflicted with human immunodeficiency virus. The varied appearance of cryptococcal skin lesion makes clinical diagnosis of cutaneous cryptococcosis difficult. Cryptococcosis proves to be a fatal fungal infection in the immunocompromised patient. Therefore, diagnosis and early treatment of cryptococcosis become vital. A 56-year-old renal transplant recipient, with an ongoing immunosuppression regimen of cyclosporine, prednisolone, and mycophenolate mofetil, was admitted with a 2-week history of pain and edema of right arm without respiratory symptoms. Despite empiric antibiotic therapy, the patient continued to complain of severe tenderness of the involved arm and fever persisted as well. On the third day of hospital stay, a biopsy of the erythematous skin lesion was acquired. On the eighth day of hospital stay, results of both skin biopsy and blood cultures showed the presence of Cryptococcus neoformans. The treatment was begun with intravenous fluconazole (400 mg/day). After 4 days of antifungal treatment, the patient developed fever along with cough with purulent sputum. As the new developing symptoms were suggestive of pneumonia, especially of pulmonary cryptococcosis, the antifungal agent was changed from fluconazole to amphotericin B treatment (0.8 mg/kg, 50 mg/day). Chest computer tomography showed improvement in the pneumonic infiltration and consolidation after 4 weeks of amphotericin B treatment. In conclusion, cellulitis in immunocompromised patients should be suspected in case of highly atypical infectious etiology, and skin biopsy should not be delayed if empiric antibiotic therapy does not control the inflammatory response. Additionally, the patient should be treated with intravenous amphotericin B treatment in case of severe cryptococcosis.


Assuntos
Humanos , Pessoa de Meia-Idade , Síndrome da Imunodeficiência Adquirida , Anfotericina B , Braço , Biópsia , Celulite (Flegmão) , Tosse , Criptococose , Cryptococcus neoformans , Ciclosporina , Edema , Febre , Fluconazol , HIV , Hospedeiro Imunocomprometido , Terapia de Imunossupressão , Transplante de Rim , Tempo de Internação , Ácido Micofenólico , Pneumonia , Prednisolona , Pele , Escarro , Tórax , Transplantes
10.
The Journal of the Korean Society for Transplantation ; : 190-193, 2013.
Artigo em Coreano | WPRIM | ID: wpr-168231

RESUMO

Ischemic steal syndrome (ISS) is one of the serious complications that can occur after construction of an arteriovenous fistula (AVF) for hemodialysis (HD). Because AVF-related ISS symptoms are usually aggravated during HD sessions, a few cases of ISS in kidney transplantation (KT) recipients have been reported in the literature. We describe a 63-year-old male with diabetic nephropathy who created AVF for maintenance HD and presented with pain at rest and tissue necrosis of the left distal fingers at 10 years post-KT. Brachial angiography revealed the presence of attenuated blood flow through the distal ulnar artery. He underwent finger amputation and AVF ligation, leading to complete relief of ischemic symptoms. The aim of this case report is to help clinicians to diagnosis a steal syndrome in kidney transplantation with a careless AVF for a long period of time.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Amputação Cirúrgica , Angiografia , Fístula Arteriovenosa , Nefropatias Diabéticas , Diagnóstico , Dedos , Transplante de Rim , Ligadura , Necrose , Diálise Renal , Artéria Ulnar
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