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Full Text Journal Articles about
Lymphocytic Interstitial Pneumonia

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Adjunctive corticosteroids may be associated with better outcome for non-HIV Pneumocystis pneumonia with respiratory failure: a systemic review and meta-analysis of observational studies.

Lin Ding, Huixue Huang, Heyan Wang, Hangyong He,

BACKGROUND:Evidence supporting corticosteroids adjunctive treatment (CAT) for Pneumocystis jirovecii pneumonia (PCP) in non-HIV patients is highly controversial. We aimed to systematically review the literature and perform a meta-analysis of available data relating to the effect of CAT on mortality of PCP in non-HIV patients. METHODS:We searched Pubmed, Medline, Embase, and ... Read more >>

Ann Intensive Care (Annals of intensive care)
[2020, 10(1):34]

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Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry-based case series.

Freerk Prenzel, Jacqueline Harfst, Nicolaus Schwerk, Frank Ahrens, Ernst Rietschel, Sabina Schmitt-Grohé, Sune M L Rubak, Krystyna Poplawska, Winfried Baden, Mandy Vogel, Sebastian Hollizeck, Julia Ley-Zaporozhan, Frank Brasch, Simone Reu, Matthias Griese, ,

OBJECTIVES:Pediatric lymphocytic interstitial pneumonia (LIP) and follicular bronchiolitis (FB) are poorly characterized lymphoproliferative disorders. We present and quantify demographics, radiological and histopathologic patterns, treatments and their responses, and outcomes in non-HIV-infected children with LIP and FB. METHODS:This structured registry-based study included a retrospective chart review, blinded analysis of imaging studies ... Read more >>

Pediatr. Pulmonol. (Pediatric pulmonology)
[2020, 55(4):909-917]

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Fulminant Acanthamoeba castellanii Encephalitis in an Ibrutinib-Treated Patient.

Jessica W Crothers, Liangge Hsu, Francisco M Marty,

We report a case of fulminant Acanthamoeba castellanii encephalitis in a patient with chronic lymphocytic leukemia treated with ibrutinib. The unusually rapid neurologic decline and fatal outcome observed are probably related to alterations in immunologic function associated with inhibition of Bruton tyrosine kinase. ... Read more >>

Open Forum Infect Dis (Open Forum Infectious Diseases)
[2020, 7(2):ofaa025]

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An SFTPC gene mutation causes childhood interstitial lung disease: first report in the Arab region.

Mohammed A Alzaid, Safa Eltahir, Muhammad Amin Ur Rahman, Wadha Alotaibi, Khalid Mobaireek,

Background:Surfactant protein C dysfunction is one of the causes of childhood interstitial lung disease but has not previously been reported in Arabian countries. Case presentation:A six-year-old girl had presented at the age of eight months old with bronchiolitis followed by a persistent cough, dyspnea and hypoxaemia. She was found to ... Read more >>

JRSM Open (JRSM open)
[2020, 11(2):2054270419894821]

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Gastric sarcoidosis: Rare revealing feature of systemic sarcoidosis.

Sayhi Sameh, Hamdi Mohamed Salah, Ghanem Mohamed, Msekni Issam, Boussetta Najah, Abid Rim, Ben Abdelhafith Nadia, Ajili Faida, Louzir Bassam,

Gastric sarcoidosis is clinically manifest in less than 1% of patients with systemic disease. Stomach is the most commonly involved site. Clinical signs are non-specific. We report the case of a female patient presenting with abdominal pain with no associated symptoms. Upper gastrointestinal endoscopy showed mucosal erosions. Biopsy and histological ... Read more >>

Arab J Gastroenterol (Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology)
[2020, :]

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Nilotinib treatment induced large granular lymphocyte expansion and maintenance of longitudinal remission in a Philadelphia chromosome-positive acute lymphoblastic leukemia.

Masao Hagihara, Jian Hua, Morihiro Inoue, Tomoyuki Uchida, Shiro Ide, Shin Ohara, Tomoiku Takaku,

It is well known that the second-generation tyrosine kinase inhibitor dasatinib evokes an immunological reaction as an off-target effect and induces large granular lymphocytes (LGLs) expansion in 30% of patients. However, LGLs expansion in nilotinib-treated patients is rare. We report the case of a 65-year-old patient with Philadelphia chromosome (Ph)-positive ... Read more >>

Int. J. Hematol. (International journal of hematology)
[2020, :]

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Video-Assisted Thoracoscopic Lung Biopsy in Critically Ill Patients With Hematologic Malignancy and Acute Respiratory Distress Syndrome: A Case Series Report.

Elizabeth Arrieta, Saveria Sangiovanni, Juan Esteban Garcia-Robledo, Mauricio Velásquez, Luz Fernanda Sua, Liliana Fernández-Trujillo,

Pulmonary complications are prevalent among patients with hematologic malignancies, who are at high risk of developing acute respiratory distress syndrome (ARDS). Although diffuse alveolar damage is considered the diagnostic hallmark of ARDS, there are plenty of other non-diffuse alveolar damage etiologies that can mimic ARDS and benefit from a specific ... Read more >>

J Investig Med High Impact Case Rep (Journal of investigative medicine high impact case reports)
[2020, 8:2324709620912101]

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GLILD Revisited: Pulmonary Pathology of Common Variable and Selective IgA Immunodeficiency.

Brandon T Larsen, Maxwell L Smith, Henry D Tazelaar, Eunhee S Yi, Jay H Ryu, Andrew Churg,

Common variable immunodeficiency (CVID) and selective immunoglobulin A deficiency (IgAD) often cause chronic lung disease, but the pulmonary pathologic features of these systemic diseases are poorly recognized by pathologists. It has been claimed that CVID cases show a characteristic combination of noncaseating granulomas-lymphoid proliferations termed granulomatous-lymphocytic interstitial lung disease (GLILD). ... Read more >>

Am. J. Surg. Pathol. (The American journal of surgical pathology)
[2020, :]

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Pulmonary Cystic Disease and Its Mimics.

Kirk D Jones,

Cystic diseases of the lung encompass a fairly broad variety of different diseases with causes including genetic abnormalities, smoking-related problems, developmental disorders, malignant neoplasms, and inflammatory processes. In addition, there are several diagnoses that closely resemble cystic lung disease, including cavitary diseases, cystic bronchiectasis, emphysema, and cystic changes in fibrosing ... Read more >>

Surg Pathol Clin (Surgical pathology clinics)
[2020, 13(1):141-163]

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A standardized postmortem protocol to assess the real burden of sudden infant death syndrome.

Stefania Rizzo, Monica De Gaspari, Elisa Carturan, Beatrice Paradiso, Donata Favretto, Gaetano Thiene, Cristina Basso,

Sudden unexpected infant death (SUID) is a major cause of death in infants < 1 year of age. Sudden infant death syndrome (SIDS) is a SUID still unexplained after post-mortem examination. In 2014, a protocol of post-mortem investigation was introduced to assess both the prevalence and the etiopathogenesis of SUID. Our aim ... Read more >>

Virchows Arch. (Virchows Archiv : an international journal of pathology)
[2020, :]

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Reply to Wand et al.: Role of Transbronchial Cryobiopsy in Interstitial Lung Diseases: An Ongoing Tale.

Arnaud Bourdin, Carey M Suehs, Thomas V Colby, Isabelle Vachier, Nicolas Molinari, Micaela Romagnoli,

Am. J. Respir. Crit. Care Med. (American journal of respiratory and critical care medicine)
[2020, 201(2):260-261]

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Diagnosis of severe respiratory infections in immunocompromised patients.

Elie Azoulay, Lene Russell, Andry Van de Louw, Victoria Metaxa, Philippe Bauer, Pedro Povoa, José Garnacho Montero, Ignacio Martin Loeches, Sangeeta Mehta, Kathryn Puxty, Peter Schellongowski, Jordi Rello, Djamel Mokart, Virginie Lemiale, Adrien Mirouse, ,

An increasing number of critically ill patients are immunocompromised. Acute hypoxemic respiratory failure (ARF), chiefly due to pulmonary infection, is the leading reason for ICU admission. Identifying the cause of ARF increases the chances of survival, but may be extremely challenging, as the underlying disease, treatments, and infection combine to ... Read more >>

Intensive Care Med (Intensive care medicine)
[2020, 46(2):298-314]

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Diffuse granulomatous disease: looking inside and outside the lungs.

Alan Williams, W Peter Kelleher, Andrew G Nicholson, Anand Devaraj, Carlos Pavesio, Felix Chua,

Thorax (Thorax)
[2020, 75(2):189-191]

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Recent advances in primary immunodeficiency: from molecular diagnosis to treatment.

Giorgia Bucciol, Isabelle Meyts,

The technological advances in diagnostics and therapy of primary immunodeficiency are progressing at a fast pace. This review examines recent developments in the field of inborn errors of immunity, from their definition to their treatment. We will summarize the challenges posed by the growth of next-generation sequencing in the clinical ... Read more >>

F1000Res (F1000Research)
[2020, 9:]

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Cutaneous microsporidiosis in an immunosuppressed patient.

Daniel A Nadelman, Ashley R Bradt, Yvonne Qvarnstrom, Cynthia S Goldsmith, Sherif R Zaki, Frank Wang, Emily H Smith, Douglas R Fullen,

Microsporidia are a group of obligate intracellular parasites that naturally infect domestic and wild animals. Human microsporidiosis is an increasingly recognized multisystem opportunistic infection. The clinical manifestations are diverse with diarrhea being the most common presenting symptom. We present a 52-year-old woman with a history of amyopathic dermatomyositis complicated by ... Read more >>

J. Cutan. Pathol. (Journal of cutaneous pathology)
[2020, :]

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Etiologic spectrum of interstitial lung diseases in Chinese children older than 2 years of age.

Xiaolei Tang, Huimin Li, Hui Liu, Hui Xu, Haiming Yang, Jinrong Liu, Shunying Zhao,

BACKGROUND:Childhood interstitial lung diseases (ILD) (chILD) refer to a rare heterogeneous group of disorders. Global collaborations have been working on the etiologies and classification scheme of chILD. With the development of medical technologies, some new diseases were identified to be associated with chILD and its etiologic spectrum is expanding. The ... Read more >>

Orphanet J Rare Dis (Orphanet journal of rare diseases)
[2020, 15(1):25]

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Follicular Bronchiolitis: Two Cases with Varying Clinical and Radiological Presentation.

Delyse Garg, Mohit Mody, Chaitanya Pal, Pratik Patel, Christina Migliore, Christine Minerowicz, Nikhil Madan,

Follicular bronchiolitis (FB) is a rare bronchiolar disorder associated with hyperplasia of the bronchial-associated lymphoid tissue (BALT). It is characterized by the development of lymphoid follicles with germinal centers in the walls of small airways. It falls under the category of lymphoproliferative pulmonary diseases (LPDs) and commonly occurs in relation ... Read more >>

Case Rep Pulmonol (Case reports in pulmonology)
[2020, 2020:4564587]

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A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity-Analysis of all Genotypes and Phenotypes.

Wen-I Lee, Wen-Lang Fan, Chun-Hao Lu, Shih-Hsiang Chen, Ming-Ling Kuo, Syh-Jae Lin, Weng-Sheng Tsai, Tang-Her Jaing, Li-Chen Chen, Kuo-Wei Yeh, Tsung-Chieh Yao, Jing-Long Huang,

The T-cell receptor (TCR)/CD3 complex is crucial for T-cell development and regulation. In humans, CD3D, CD3E, and CD3Z gene defects cause severe combined T- and B-cell immunodeficiency. However, CD3G mutations alone lead to a less severe condition, which is mainly characterized by autoimmunity. In the present study, we report the ... Read more >>

Front Immunol (Frontiers in immunology)
[2019, 10:2833]

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Non-infectious Complications of Common Variable Immunodeficiency: Updated Clinical Spectrum, Sequelae, and Insights to Pathogenesis.

Hsi-En Ho, Charlotte Cunningham-Rundles,

Non-infectious complications in common variable immunodeficiency (CVID) have emerged as a major clinical challenge. Detailed clinical spectrum, organ-specific pathologies and associated sequelae from 623 CVID patients followed in New York since 1974 were analyzed, and recent insights to pathogenesis were reviewed. Non-infectious manifestations were present in 68.1% of patients, and ... Read more >>

Front Immunol (Frontiers in immunology)
[2020, 11:149]

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Recurrent pneumothorax, skin lesions and frequent urination.

Kunal Deokar, Ram Niwas, Nishant Chauhan, Naveen Dutt, Priyank Jain, Shahir Asfahan, Rajani Kumawat,

The causes of cystic lung diseases are varied. Proper evaluation is required for appropriate management. http://bit.ly/37J7dvE. ... Read more >>

Breathe (Sheff) (Breathe (Sheffield, England))
[2020, 16(1):190318]

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Rituximab as a Single Agent for Granulomatous Lymphocytic Interstitial Lung Disease in Common Variable Immune Deficiency.

G Tessarin, M P Bondioni, S Rossi, L Palumbo, A Soresina, R Badolato, A Plebani, V Lougaris,

J Investig Allergol Clin Immunol (Journal of investigational allergology & clinical immunology)
[2019, 29(6):470-471]

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Lymphocytic interstitial pneumonia and pulmonary amyloidosis in Sjögren's syndrome.

Eurípedes Barsanulfo de Paula Avelino, Leonardo Verza, Tércia Neves, Rubens Chojniak, Marcos Duarte Guimarães,

Radiol Bras (Radiologia brasileira)
[2019, 52(6):410-411]

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An unusual mimicker of asthma in an active duty army physician: Common variable immunodeficiency presenting as granulomatous lymphocytic interstitial lung disease.

Cpt Cyrus Askin, Maj Jean Coviello, Maj Justin Reis,

Active duty service members are frequently diagnosed with asthma after referral to pulmonary for undifferentiated cough and dyspnea. Occasionally, patients have symptoms despite optimal therapy necessitating evaluation for asthma mimickers. We present a 48 year-old active duty physician who initially presented in 2007 with dyspnea and cough. Despite the absence ... Read more >>

Respir Med Case Rep (Respiratory medicine case reports)
[2020, 29:100965]

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A Rare Combination of Gastric Mucosa-associated Lymphoid Tissue Lymphoma, Autoimmune Gastritis, Thyroiditis, Hemolysis, and Systemic Lupus Erythematosus.

Tohru Kotera, Katsuhiko Itani, Hitoji Uchiyama, Takahiro Takemoto, Kazue Ooyama, Kuniaki Hirata, Shinsaku Imashuku, Shigemi Nakajima,

We herein report a case with the rare combination of mucosa-associated lymphoid tissue lymphoma (MALT lymphoma) of the stomach, autoimmune gastritis (AIG), autoimmune thyroiditis, autoimmune hemolytic anemia (AIHA), and systemic lupus erythematosus. A 68-year-old woman was diagnosed with gastric MALT lymphoma associated with Helicobacter pylori (H. pylori) infection and AIG. ... Read more >>

Intern. Med. (Internal medicine (Tokyo, Japan))
[2020, 59(1):61-65]

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Hydroxychloroquine is associated with a lower risk of polyautoimmunity: data from the RELESSER Registry.

Natalia Mena-Vázquez, Antonio Fernández-Nebro, José María Pego-Reigosa, María Galindo, Ana Melissa-Anzola, Esther Uriarte-Isacelay, Alejandro Olivé-Marqués, Elena Aurrecoechea, Mercedes Freire, Eva Tomero, María Jesús García-Villanueva, Claudia Stoye, Esteban Salas-Heredia, Jose Antonio Bernal-Vidal, Eva Salgado, Ricardo Blanco, Francisco Javier Novoa, Mónica Ibáñez-Barcelo, Vicente Torrente-Segarra, Javier Narvaez, Joan Calvet, Clara Moriano Morales, Tomas Ramon Vazquez-Rodriguez, Paloma Garcia de la Peña, Cristina Bohórquez, José Luis Andreu-Sánchez, Tatiana Cobo-Ibañez, Gema Bonilla, Nuria Lozano-Rivas, Carlos Montilla, Francisco Javier Toyos, Jose Luis Marenco De la Fuente, Lorena Expósito, María Esther Ruiz-Lucea, Elia Vals, Javier Manero-Ruiz, Jose A Bernal-Vidal, Iñigo Rua-Figueroa,

OBJECTIVES:This article estimates the frequency of polyautoimmunity and associated factors in a large retrospective cohort of patients with SLE. METHODS:RELESSER (Spanish Society of Rheumatology Lupus Registry) is a nationwide multicentre, hospital-based registry of SLE patients. This is a cross-sectional study. The main variable was polyautoimmunity, which was defined as the ... Read more >>

Rheumatology (Oxford) (Rheumatology (Oxford, England))
[2019, :]

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