scholarly journals A Fatal Extrapulmonary Manifestation of COVID-19

Cureus ◽  
2021 ◽  
Author(s):  
Chad L Harris ◽  
Supraja Achuthanandan ◽  
Kiran Para ◽  
Vijay Shetty
Keyword(s):  
Extrapulmonary Manifestation

scholarly journals An extrapulmonary manifestation of lymphangioleiomyomatosis: A rare case report

2017 ◽  
Vol 41 ◽  
pp. 315-318
Author(s):  
L. Volkan Tümay ◽  
Osman Serhat Güner ◽  
Abdullah Zorluoğlu
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
Extrapulmonary Manifestation

scholarly journals Suspected Acute Abdomen as an Extrapulmonary Manifestation of Covid-19 Infection

2020 ◽  
Vol 98 (5) ◽  
pp. 295-296
Author(s):  
Ruth Blanco-Colino ◽  
Ramon Vilallonga ◽  
Rocío Martín ◽  
Carlos Petrola ◽  
Manuel Armengol
Keyword(s):  
Acute Abdomen ◽  
Extrapulmonary Manifestation

scholarly journals Imaging of compound palmar ganglion with pathologic correlation

2014 ◽  
Vol 18 (1) ◽  
Author(s):  
Sourav Talukder ◽  
Anindya Bandyopadhay ◽  
Shamick Biswas ◽  
Sumit Chakraborty ◽  
Suchismita Chakrabarti
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Imaging Features ◽  
Resonance Imaging ◽  
Common Site ◽  
Radiological Features ◽  
Flexor Tenosynovitis ◽  
Compound Palmar Ganglion ◽  
Extrapulmonary Manifestation ◽  
Palmar Aspect

Compound palmar ganglion, or chronic flexor tenosynovitis, most commonly of tuberculousorigin, is a rare extrapulmonary manifestation of tuberculosis (TB). The flexor synovialsheath is not a common site for TB but, once involved, causes rapid involvement of all flexortendons. We discuss the case of a 70-year-old farmer who presented to us with pain and progressive swelling of the palmar aspect of the wrist. On clinical examination, swelling both above and below the proximal wrist crease was found, with positive cross-fluctuation. Onultrasonography and magnetic resonance imaging, features suggestive of compound palmarganglion were present. The patient underwent surgical resection (extensive tenosynovectomy)and chemotherapy. Post-operative histopatholgical findings correlated with the radiological features.

scholarly journals EXTRAPULMONARY MANIFESTATION OF SARCOIDOSIS ASSOCIATED WITH AUTOIMMUNE HEMOLYTIC ANEMIA (AIHA)

2021 ◽  
Author(s):  
Iane Tamara Dondé ◽  
Viviane Queiroz de Oliveira Maia ◽  
Danielly Dantas Pimentel ◽  
Gizelle Gouvea Rezende ◽  
Gustavo Roberto Lourenço ◽  
...  
Keyword(s):  
Hemolytic Anemia ◽  
Autoimmune Hemolytic Anemia ◽  
Extrapulmonary Manifestation

scholarly journals Extrapulmonary manifestation of lymphangioleiomyomatosis.

2015 ◽  
Vol 98 (1) ◽  
pp. 53
Author(s):  
N. Favoreel ◽  
S. F. Van Meerbeeck ◽  
R. Gosselin
Keyword(s):  
Extrapulmonary Manifestation

scholarly journals POTT DISEASE IN IMMUNOSUPPRESSED PATIENT, A CASE REPORT.

2020 ◽  
Vol 7 (1) ◽  
pp. 52-54
Author(s):  
Heloyse Nascimento Lima ◽  
Romulo Braga Pires ◽  
Angelica Gomes de Carvalho ◽  
Isabella Vilane Braga Saboia Rythowem ◽  
Pedro Miranda Portugal Junior ◽  
...  
Keyword(s):  
Symptomatic Improvement ◽  
Lower Limbs ◽  
Immunosuppressed Patient ◽  
Rare Entity ◽  
Good Clinical Outcome ◽  
Pott’S Disease ◽  
Night Sweats ◽  
Immunosuppressed Patients ◽  
History Of ◽  
Extrapulmonary Manifestation

Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis. The pulmonary form is more frequent, but other body structures may be affected. Pott's Disease is a rare entity and accounts for about 0.5% - 1% of extrapulmonary manifestation, especially in immunosuppressed patients. It occurs through reactivation of sites for the spine and sometimes lower limbs. The symptomatology presents itself through the triad: abscess, paraplegia and gibbosity, associated with the classic clinical picture of pulmonary TB: fever, night sweats and chills. The aim of this study is to demonstrate a case of Pott's disease in a 56-year-old female patient with a history of chemotherapy due to non-Hodgkin's lymphoma. After treatment, the patient evolved with symptomatic improvement and good clinical outcome.

scholarly journals A case of granulomatous tubulointerstitial nephritis in a patient with pulmonary sarcoidosis

2020 ◽  
Vol 92 (6) ◽  
pp. 81-83
Author(s):  
Leonid I. Dvoretsky ◽  
Sergei A. Krivushkin ◽  
Ekaterina S. Stolyarevich ◽  
Elizaveta A. Skrynnikova ◽  
Andrey P. Stepanchenko ◽  
...  
Keyword(s):  
Renal Failure ◽  
Chronic Renal Failure ◽  
Renal Biopsy ◽  
Replacement Therapy ◽  
Clinical Observation ◽  
Tubulointerstitial Nephritis ◽  
Pulse Therapy ◽  
Pulmonary Sarcoidosis ◽  
Interstitial Tissue ◽  
Extrapulmonary Manifestation

A clinical observation is presented of a patient with pulmonary sarcoidosis, who was diagnosed with kidney damage after three years with the development of chronic renal failure and the need for replacement therapy. A histological examination of the renal biopsy revealed a granulomatous process in the interstitial tissue, which was regarded as an extrapulmonary manifestation of sarcoidosis. Pulse therapy with glucocorticoids was prescribed and an attempt was made to reduce hemodialysis sessions.

Symptomatic nodular myopathy: an atypical presentation of sarcoidosis

2021 ◽  
Vol 14 (5) ◽  
pp. e241206
Author(s):  
Mostafa Ellatif ◽  
Parthdev Bhasin ◽  
Carlo Urigo ◽  
Ajay Sahu
Keyword(s):  
Soft Tissue ◽  
Literature Review ◽  
Multidisciplinary Approach ◽  
Multimodality Imaging ◽  
Radiology Department ◽  
Atypical Presentation ◽  
Imaging Characteristics ◽  
Short Period ◽  
History Of ◽  
Extrapulmonary Manifestation

Symptomatic myopathy is a very rare extrapulmonary manifestation of sarcoidosis that may not be readily recognised in the absence of a known history of sarcoid. Nodular myopathy is the most uncommon subtype of musclar sarcoidosis and, when encountered, establishing the diagnosis can be challenging. We present a case of symptomatic nodular myopathy as a first presentation of sarcoidosis in a young man who required a multidisciplinary approach to diagnose. The patient presented to our radiology department following a short period of flu-like illness and multiple soft tissue lesions. Biopsy of the lesions demonstrated noncaseating granulomata, and a diagnosis of sarcoidosis was established after important differential diagnoses were excluded. We present a literature review of sarcoid-related myopathy and the multimodality imaging characteristics of the different subtypes.

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