scholarly journals Case report of mild form of a new coronavirus infection in patient with idiopathic pulmonary hypertension

Kardiologiia ◽  
2021 ◽  
Vol 61 (10) ◽  
pp. 108-112
Author(s):  
S. E. Gratsianskaya ◽  
A. Yu. Demchenkova ◽  
T. V. Martynyuk ◽  
T. N. Veselova ◽  
S. K. Ternovoy
Keyword(s):  
Pulmonary Hypertension ◽  
Case Report ◽  
Female Patient ◽  
Interstitial Pneumonia ◽  
Clinical Case ◽  
Mild Form ◽  
Idiopathic Pulmonary Hypertension ◽  
Coronavirus Infection ◽  
Novel Coronavirus

The article presents a clinical case of mild novel coronavirus infection COVID-19 complicated with bilateral interstitial pneumonia in a female patient with idiopathic pulmonary hypertension. 

scholarly journals Mediastinal Emphysema as a Specific Complication of COVID-19 (Case Report)

2021 ◽  
Vol 17 (2) ◽  
pp. 4-15
Author(s):  
E. P. Pavlikova ◽  
M. A. Agapov ◽  
P. S. Malakhov ◽  
E. A. Galliamov ◽  
Yu. S. Esakov ◽  
...  
Keyword(s):  
Case Report ◽  
Clinical Case ◽  
Lung Ventilation ◽  
Mediastinal Emphysema ◽  
The Novel ◽  
Spontaneous Pneumomediastinum ◽  
Specific Complication ◽  
Coronavirus Infection ◽  
Research And Education ◽  
Novel Coronavirus

During the care of patients with novel coronavirus infection at the Lomonosov MSU Medical Research and Education Center from April 21 to June 13, 2020, we observed cases of spontaneous mediastinal emphysema (spontaneous pneumomediastinum) as a manifestation or a probable complication of COVID-19.The aim of the paper. To provide clinical case descriptions and approaches to the management of patients with spontaneous pneumomediastinum in COVID-19 associated pneumonia, as they are not addressed in the current clinical guidelines, and therefore are worthy of special attention.Among 224 patients with laboratory-confirmed diagnosis of the novel coronavirus infection COVID-19, five cases of pneumomediastinum without pneumothorax were identified. Of these, in two cases the pneumomediastinum developed during noninvasive lung ventilation (NLV) (one case) and invasive lung ventilation (one case). In three cases, spontaneous mediastinal emphysema was not associated with lung ventilation. By the time of publication, one case of pneumomediastinum was completed, and four patients remained hospitalized. All five patients were males aged from 52 to 84 years.This paper presents in depth the description of two cases of mediastinal and subcutaneous emphysema in patients with COVID-19.

scholarly journals A clinical case of long-term macitentan therapy in a female patient with idiopathic pulmonary hypertension

2016 ◽  
Vol 88 (12) ◽  
pp. 88-93 ◽  
Author(s):  
O A Arkhipova ◽  
T V Martynyuk ◽  
I E Chazova
Keyword(s):  
Pulmonary Hypertension ◽  
Female Patient ◽  
Clinical Case ◽  
Endothelin Receptor ◽  
Pathogenetic Therapy ◽  
Pulmonary Arterial ◽  
Idiopathic Pulmonary Hypertension ◽  
The Russian Federation ◽  
The Given

In late 2015, the Russian Federation registered the new non-selective endothelin receptor antagonist macitentan for the pathogenetic therapy of pulmonary arterial hypertension. The given clinical case demonstrates the possibility of using macitentan in a female patient with idiopathic pulmonary hypertension and its ability to affect the clinical, hemodynamic, and functional status of patients and to slow down the progression of the disease.

scholarly journals New coronavirus infection COVID-19 as a trigger for the development of symptoms of ankylosing spondylitis. Case report

2021 ◽  
Vol 93 (5) ◽  
Author(s):  
Daria G. Rumiantceva ◽  
Margarita M. Urumova ◽  
Shandor F. Erdes
Keyword(s):  
Back Pain ◽  
Case Report ◽  
Ankylosing Spondylitis ◽  
Clinical Case ◽  
Inflammatory Back Pain ◽  
The Novel ◽  
Coronavirus Infection ◽  
Novel Coronavirus ◽  
Positive Effect

The novel coronavirus infection COVID-19 (SARS-CoV-2) is now known to cause a variety of extrapulmonary complications, including cardiovascular, neurological and dermatological complications, many of which occur or last several weeks after infection. We present a clinical case of a patient who first developed symptoms of ankylosing spondylitis 2 weeks after recovering from COVID-19. The patient was prescribed therapy in accordance with international and Russian recommendations for the management of patients with ankylosing spondylitis with a positive effect in the form of absence arthritis, enthesitis and reducing the inflammatory back pain.

The novel coronavirus infection (COVID-19) concurrent with pseudomembranous colitis in the early postpartum period: a clinical case

2021 ◽  
Vol 9_2021 ◽  
pp. 232-236
Author(s):  
Shklyaev A.E. Shklyaev A ◽  
Bessonov A.G. Bessonov A ◽  
Chushyalova D.A. Chushyalova D ◽  
Mikhailova M.D. Mikhailova M ◽  
Meleshkina M.V. Meleshkina M ◽  
...  
Keyword(s):  
Postpartum Period ◽  
Pseudomembranous Colitis ◽  
Clinical Case ◽  
The Novel ◽  
Early Postpartum Period ◽  
Early Postpartum ◽  
Coronavirus Infection ◽  
Novel Coronavirus

scholarly journals Diffuse Oligosymptomatic Caroli’s Disease: Case Report

2020 ◽  
Vol 31 (2) ◽  
pp. 107-110
Author(s):  
Lemfadli Y ◽  
Bouchrit S ◽  
Ait Errami A ◽  
Oubaha S ◽  
Samlani Z ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Bile Ducts ◽  
Clinical Case ◽  
Caroli's Disease ◽  
Caroli’S Disease ◽  
Caroli Disease ◽  
Intrahepatic Bile Ducts ◽  
Disease Case

This article describes a case of Caroli’s disease in a 53-year-old female patient who complained nonspecificabdominal pain without cholestasis or cholangitis. Ultrasound and hepatic magnetic resonanceimaging showed segmental saccular dilations connected to intrahepatic bile ducts without hepaticfibrosis. This clinical case shows the possibility of having oligosymptomatic forms in the diffuse formsof Caroli disease, therefore the interest to consider this diagnosis in case of non-specific abdominalsigns and to request a hepatic ultrasound. Bangladesh J Medicine July 2020; 31(2) : 107-110

scholarly journals Interventional Treatment of Lymphatic Leakage Post Appendectomy: Case Report

2019 ◽  
Vol 7 (9) ◽  
pp. 1512-1515
Author(s):  
Nguyen Ngoc Cuong ◽  
Nguyen Thai Binh ◽  
Phan Nhan Hien ◽  
Nguyen Hoang ◽  
Le Tuan Linh ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Case ◽  
Iliac Fossa ◽  
Chylous Ascites ◽  
Percutaneous Intervention ◽  
Interventional Treatment ◽  
Lymphatic Complications ◽  
The Right ◽  
Intranodal Lymphangiography

BACKGROUND: Postoperative lymphatic complications are not common, and lymphatic leakage complication post appendectomy (LLCPC) is even rarer. However, the number of this operation is high so LLCPC can occur. CASE REPORT: Here, we report a female patient post appendectomy with severe chylous ascites. This patient underwent six operations. A leakage point at the right iliac-fossa, which was embolized successfully after two sessions, was spotted during intranodal lymphangiography. After 6 months, the ascites were significantly reduced while some lymphatic aneurysms still existed in the lumbar-retroperitoneal region. CONCLUSIONS: Basing the knowledge of this clinical case and literature, we have concluded that lymphatic leakage can be diagnosed and embolized by percutaneous intervention.

scholarly journals A clinical case of chickenpox complicated by meningoencephalitis and cerebral edema in combination with a novel coronavirus infection (COVID-19) in a 5-year-old child

2021 ◽  
Vol 20 (2) ◽  
pp. 64-67
Author(s):  
M. N. Kuzmina ◽  
E. G. Klimovitskaya ◽  
S. N. Eshmolov ◽  
I. G. Sitnikov ◽  
E. V. Elyakova
Keyword(s):  
Infectious Diseases ◽  
Cerebral Edema ◽  
Blood Test ◽  
Clinical Case ◽  
Neurological Symptoms ◽  
Immune Reactivity ◽  
Mucous Membranes ◽  
Coronavirus Infection ◽  
Novel Coronavirus ◽  
Inflammatory Changes

The new coronavirus infection COVID-1 9 in children generally proceeds favorably, but in combination with other acute infectious diseases and in persons with background pathology and impaired immune reactivity may pose a particular threat.The article presents a clinical case of chickenpox, complicated by meningoencephalitis and cerebral edema, in combination with COVID-1 9 in a 5-year-old child. Chickenpox was not quite typical: against the background of febrile temperature, there was a scanty spot-papular rash with single vesicles that appeared later, the absence of elements on the mucous membranes and the development of neurological symptoms in the first day of the disease. CОVID-1 9 was characterized by a wave-like course with fever up to 39,1 °C, tonsillitis phenomena and inflammatory changes in the blood test.

Clinical case of idiopathic pulmonary hypertension complicated by thrombosis in situ (9-year follow-up)

2021 ◽  
Vol 22 (2) ◽  
pp. 93-97
Author(s):  
D. F. Nizamova ◽  
◽  
Z. M. Safiullina ◽  
O. V. Abaturova ◽  
O. V. Kremneva ◽  
...  
Keyword(s):  
Pulmonary Hypertension ◽  
Differential Diagnosis ◽  
Clinical Case ◽  
Disease Development ◽  
Pathogenetic Mechanisms ◽  
Idiopathic Pulmonary Hypertension

The article presents a clinical case of idiopathic pulmonary hypertension complicated by thrombosis in situ (9-year follow-up). Possible pathogenetic mechanisms of the disease development are analyzed. The difficulties of differential diagnosis and the treatment of idiopathic pulmonary hypertension are discussed.

Development of lymphangioleiomyomatosis in a female patient with Sjö gren's disease: a review of literature and a case report

2019 ◽  
Vol 13 (2) ◽  
pp. 119-123
Author(s):  
Yu. I. Khvan ◽  
S. G. Palshina ◽  
V. I. Vasiliev
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Case ◽  
Young Female ◽  
Renal Angiomyolipoma ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
History Of ◽  
Genetically Determined ◽  
Sjögren’S Disease

Cystic and bullous lung transformation occurs in diseases of various origins: neoplastic, genetically determined, rheumatic, lymphoproliferative, and infectious diseases. The paper presents a review of the literature and a clinical case of a young female patient with a long history of Sjögren's disease. Fifteen years after the onset of the disease, the patient developed cystic and bullous lung transformation and renal angiomyolipoma, which are regarded as a manifestation of probable lymphangioleiomyomatosis.

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