706 results match your criteria Imaging in Hypertrophic Osteoarthropathy


Spectrum of Voriconazole-Induced Periostitis With Review of the Differential Diagnosis.

AJR Am J Roentgenol 2019 Jan 7;212(1):157-165. Epub 2018 Nov 7.

1 Department of Radiology, University of Illinois College of Medicine, 1740 W Taylor St, Rm. 2483 (MC 931), Chicago, IL 60612.

Objective: Voriconazole is an antifungal medication used primarily for the treatment of Candida and Aspergillus infections. A fairly newly described side effect of long-term voriconazole use is periostitis. The purpose of this article is to describe the main differential consideration-hypertrophic osteoarthropathy-and other differential diagnoses, including venous stasis, thyroid acropachy, and hypervitaminosis A. Read More

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https://www.ajronline.org/doi/10.2214/AJR.18.19991
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http://dx.doi.org/10.2214/AJR.18.19991DOI Listing
January 2019
17 Reads

A Case of Hypertrophic Pulmonary Osteoarthropathy in Both Upper and Lower Extremities: A Rare Involvement.

Mol Imaging Radionucl Ther 2018 Jun;27(2):88-90

Ankara Numune Training and Research Hospital, Clinic of Nuclear Medicine, Ankara, Turkey.

Hypertrophic pulmonary osteoarthropathy (HPOA) is a paraneoplastic manifestation of gastric and, more frequently, lung carcinomas. It is characterized by extremity pain, clubbing, arthritis and periostitis of the long bones. Periostitis is the hallmark of HPOA and can be revealed with bone scintigraphy. Read More

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http://dx.doi.org/10.4274/mirt.78941DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996602PMC
June 2018
13 Reads

Proliferative Periostitis – eine seltene Differenzialdiagnose.

Rofo 2018 May 18;190(5):450-453. Epub 2018 Jan 18.

Diagnostic Radiology, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

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http://dx.doi.org/10.1055/s-0043-125220DOI Listing
May 2018
14 Reads

Hypertrophic Osteoarthropathy on Bone Scintigraphy.

J Nucl Med Technol 2018 Jun 10;46(2):147-148. Epub 2017 Nov 10.

Department of Diagnostic Radiology and Molecular Imaging, Oakland University and Beaumont Hospital, Royal Oak, Michigan.

We present the case report of a patient with a history of lung cancer in whom the typical pattern of hypertrophic osteoarthropathy was seen on bone scintigraphy. We discuss the etiologies, pathophysiology, and management of this entity. Read More

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http://dx.doi.org/10.2967/jnmt.117.199315DOI Listing
June 2018
19 Reads

Pachydermoperiostosis: The value of molecular diagnosis.

Ann Dermatol Venereol 2017 Dec 12;144(12):799-803. Epub 2017 Sep 12.

Department of Dermatology, hôpital Saint-Louis, AP-HP, 1, avenue Claude-Vellefaux, 75475 Paris cedex 10, France; MAGEC, hôpital Saint-Louis, AP-HP, 1, avenue Claude-Vellefaux, 75475 Paris cedex 10, France. Electronic address:

Background: Pachydermoperiostosis is a rare autosomal recessive genetic disorder characterized by the association of periostosis and pachydermia. To date, two genes involved in prostaglandin metabolism, HPGD and SLCO2A1, have been identified.

Patients And Methods: A 7-year-old girl presented digital clubbing of the hands and feet, curved nails, hyperhidrosis, and pachydermia, as well as eczema of the trunk and limbs. Read More

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http://dx.doi.org/10.1016/j.annder.2017.03.027DOI Listing
December 2017
25 Reads

Secondary hypertrophic osteoarthropathy caused by non-pleural or pulmonary tumors.

Medicine (Baltimore) 2017 Sep;96(36):e7985

aDepartment of Diagnostic and Interventional Radiology, University Hospital Leipzig, Leipzig bDepartment of Diagnostic Radiology, Martin-Luther University Halle (Saale), Halle (Saale), Germany.

Hypertrophic osteoarthropathy (HOA) is a rare paraneoplastic syndrome characterized by digital clubbing, periosteal reaction, polyarthralgia, arthritis, and synovitis. Herein, we report a case series of patients with secondary HOA caused by non-pleural or pulmonary tumors.The radiologic databases of 2 tertiary university hospitals were retrospectively screened for secondary HOA patients. Read More

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http://dx.doi.org/10.1097/MD.0000000000007985DOI Listing
September 2017
31 Reads

A smoker with joint pain.

BMJ 2017 07 20;358:j3149. Epub 2017 Jul 20.

Great Western Hospital NHS Foundation Trust, Great Western Hospital, Swindon, UK.

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http://dx.doi.org/10.1136/bmj.j3149DOI Listing
July 2017
9 Reads

Voriconazole-Induced Periostitis Deformans: A Mimicker of Hypertrophic Pulmonary Osteoarthropathy.

Clin Med Res 2017 Jun 9;15(1-2):19-20. Epub 2017 May 9.

Professor of Medicine, University of Toronto, Rheumatology Department, Toronto, Canada.

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http://dx.doi.org/10.3121/cmr.2017.1357DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573518PMC
June 2017
7 Reads

You're the Flight Surgeon.

Authors:

Aerosp Med Hum Perform 2017 May;88(5):511-515

Chumbley EM. You're the flight surgeon: a case of bilateral leg pain and swelling in a loadmaster. Aerosp Med Hum Perform. Read More

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http://dx.doi.org/10.3357/AMHP.4810.2017DOI Listing
May 2017
8 Reads

Hypertrophic osteoarthropathy: Uncommon presentation of lung cancer.

Cleve Clin J Med 2017 Apr;84(4):270-272

Professor and Head of the Department, Institute of Chest Diseases, Government Medical College, Kozhikode, Kerala, India.

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http://dx.doi.org/10.3949/ccjm.84a.15167DOI Listing
April 2017
1 Read

Graft Infection Masquerading as Rheumatologic Disease: a Rare Case of Aortobifemoral Graft Infection Presenting as Hypertrophic Osteoarthropathy.

Ann Vasc Surg 2017 May 7;41:283.e11-283.e18. Epub 2017 Mar 7.

Division of Infectious Disease, Departments of Vascular Surgery and Internal Medicine, Mercy Health Saint Mary's Hospital, Grand Rapids, MI. Electronic address:

Background: Prosthetic vascular graft procedures are a common treatment modality for peripheral vascular disease. A relatively common complication is graft infection, occurring at a rate of 0.5-5%. Read More

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http://dx.doi.org/10.1016/j.avsg.2016.10.041DOI Listing
May 2017
11 Reads

A rare cause of digital clubbing: pachydermoperiostosis.

Pan Afr Med J 2016;25:194. Epub 2016 Nov 25.

Department of Orthopaedics, Sahloul Hospital, Faculty of Medicine of Sousse, Sousse, Tunisia.

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http://dx.doi.org/10.11604/pamj.2016.25.194.10890DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5326264PMC
February 2018
13 Reads

[Genetic analysis of a pedigree with primary hypertrophic osteoarthropathy].

Zhonghua Nei Ke Za Zhi 2017 Mar;56(3):194-198

Department of Endocrinology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450000, China.

To analyze the clinical and genetic features of primary hypertrophic osteoarthropathy (PHO). The clinical data of one Chinese pedigree of PHO, namely pachydermoperiostosis (PDP) were collected.Blood samples were drawn from the propositus and other family members. Read More

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http://dx.doi.org/10.3760/cma.j.issn.0578-1426.2017.03.009DOI Listing
March 2017
5 Reads

A rare case of pachydermoperiostosis associated with blepharoptosis and floppy eyelids.

Indian J Ophthalmol 2016 Dec;64(12):938-940

Department of Orbit Oculoplasty Reconstructive and Aesthetic Services, Sankara Nethralaya, Medical Research Foundation, Chennai, Tamil Nadu, India.

Pachydermoperiostosis (PDP) is a multisystem disorder of mesenchymal origin. It is a form of hypertrophic osteoarthropathy. The typical clinical features include pachydermia, cutis verticus gyrata, digital clubbing, and periostosis. Read More

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http://dx.doi.org/10.4103/0301-4738.198865DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322714PMC
December 2016
14 Reads

Hypertrophic Osteoarthropathy Secondary to Lung Cancer: Beneficial Effect of Anti-vascular Endothelial Growth Factor Antibody.

J Clin Rheumatol 2017 Jan;23(1):47-50

Department of Respiratory Medicine Tokyo Medical University Ibaraki Medical Center 3-20-1 Chuou, Ami, Inashiki Ibaraki 300-0395, Japan

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http://dx.doi.org/10.1097/RHU.0000000000000441DOI Listing
January 2017
18 Reads

Hypertrophic Osteoarthropathy: Clinical and Imaging Features.

Radiographics 2017 Jan-Feb;37(1):157-195. Epub 2016 Dec 9.

From the Department of Radiology, Keck School of Medicine, University of Southern California, 1500 San Pablo St, 2nd Floor Imaging, Los Angeles, CA 90033 (F.Y.Y., D.B.P., A.J.S., E.A.W., A.T., G.R.M.); Department of Radiology, Southern California University of Health Sciences, Whittier, Calif (M.R.S.); and Department of Radiology, Greater Los Angeles Veterans Affairs Medical Center, Los Angeles, Calif (S.M.).

Hypertrophic osteoarthropathy (HOA) is a medical condition characterized by abnormal proliferation of skin and periosteal tissues involving the extremities and characterized by three clinical features: digital clubbing (also termed Hippocratic fingers), periostosis of tubular bones, and synovial effusions. HOA can be a primary entity, known as pachydermoperiostosis, or can be secondary to extraskeletal conditions, with different prognoses and management implications for each. There is a high association between secondary HOA and malignancy, especially non-small cell lung cancer. Read More

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http://dx.doi.org/10.1148/rg.2017160052DOI Listing
September 2017
44 Reads
2.602 Impact Factor

FGF2 High Molecular Weight Isoforms Contribute to Osteoarthropathy in Male Mice.

Endocrinology 2016 Dec 12;157(12):4602-4614. Epub 2016 Oct 12.

Department of Medicine, Division of Endocrinology and Metabolism, School of Medicine (P.M.B., L.X., M.M.H.), and Department of Reconstructive Sciences Center for Regenerative Medicine and Skeletal Development, School of Dental Medicine (C.D.), UConn Health, Farmington, CT, 06030-3023.

Humans with X-linked hypophosphatemia (XLH) and Hyp mice, the murine homolog of the disease, develop severe osteoarthropathy and the precise factors that contribute to this joint degeneration remain largely unknown. Fibroblast growth factor 2 (FGF2) is a key regulatory growth factor in osteoarthritis. Although there are multiple FGF2 isoforms the potential involvement of specific FGF2 isoforms in joint degradation has not been investigated. Read More

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http://dx.doi.org/10.1210/en.2016-1548DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133359PMC
December 2016
13 Reads

Hypertrophic Osteoarthropathy: an Unusual Cause of Knee Pain and Recurrent Effusion.

HSS J 2016 Oct 30;12(3):284-286. Epub 2016 Aug 30.

Department of Orthopaedic Surgery, Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021 USA.

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http://dx.doi.org/10.1007/s11420-016-9522-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026666PMC
October 2016
17 Reads

Joint effusion as an indication of a lung disease.

Eur J Intern Med 2016 Dec 18;36:e5-e6. Epub 2016 Aug 18.

Department of Orthopedics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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http://dx.doi.org/10.1016/j.ejim.2016.08.004DOI Listing
December 2016
3 Reads

Poorly Differentiated Neuroendocrine Tumor of the Esophagus with Hypertrophic Osteoarthropathy and Brain Metastasis: A Success Story.

Cureus 2016 Jun 19;8(6):e646. Epub 2016 Jun 19.

Medicine, Tufts Medical Center.

Neuroendocrine carcinomas (NECs) of the esophagus are very rare. The majority of the patients with NECs present with metastasis. Paraneoplastic syndromes, such as syndrome of inappropriate secretion of anti-diuretic hormone and watery diarrhea-hypokalemia-achlorhydria syndrome, have been reported in previous reports. Read More

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http://dx.doi.org/10.7759/cureus.646DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4954639PMC
June 2016
13 Reads

Identification of the Mutations in the Prostaglandin Transporter Gene, SLCO2A1 and Clinical Characterization in Korean Patients with Pachydermoperiostosis.

J Korean Med Sci 2016 May 22;31(5):735-42. Epub 2016 Mar 22.

Department of Internal Medicine, Endocrine Research Institute, Yonsei University College of Medicine, Seoul, Korea .

Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare genetic disease affecting both skin and bones. Both autosomal dominant with incomplete penetrance and recessive inheritance of PDP have been previously confirmed. Recently, hydroxyprostaglandin dehydrogenase (HPGD) and solute carrier organic anion transporter family member 2A1 (SLCO2A1) were reported as pathogenic genes responsible for PDP. Read More

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http://dx.doi.org/10.3346/jkms.2016.31.5.735DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835599PMC
May 2016
18 Reads

Painful and swollen hands 3 months after lungs graft: Suracute voriconazole-induced periostitis and exostosis.

Joint Bone Spine 2017 Jan 23;84(1):97-98. Epub 2016 Apr 23.

Rheumatology unit, Hôtel-Dieu, Nantes university hospital, CHU de Nantes, place Alexis-Ricordeau, 44093 Nantes cedex, France. Electronic address:

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http://dx.doi.org/10.1016/j.jbspin.2015.11.011DOI Listing
January 2017
12 Reads

[Digital clubbing in pulmonary veno-occlusive disease].

Med Clin (Barc) 2016 Oct 6;147(8):379. Epub 2016 Mar 6.

Unidad de Insuficiencia Cardiaca, Trasplante Cardiaco e Hipertensión Pulmonar, Departamento de Cardiología, Hospital Universitario 12 de Octubre, Madrid, España.

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http://dx.doi.org/10.1016/j.medcli.2016.01.020DOI Listing
October 2016
41 Reads

Primary hypertrophic osteoarthropathy: ultrasound and MRI findings.

Pediatr Radiol 2016 May 3;46(5):727-30. Epub 2016 Mar 3.

Clarendon Wing Radiology Department, Leeds Children's Hospital at The Leeds General Infirmary, Belmont Grove, Leeds, West Yorkshire, UK, LS2 9NS.

Primary hypertrophic osteoarthropathy is a rare genetic disorder related to failures in prostaglandin metabolism. Patients present with joint pain, limb enlargement, skin thickening and finger clubbing. Radiographs show characteristic periosteal reaction and thickening along the long bones. Read More

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http://dx.doi.org/10.1007/s00247-016-3544-8DOI Listing
May 2016
11 Reads

Pseudoacromegaly in pachydermoperiostosis.

BMJ Case Rep 2016 Feb 17;2016. Epub 2016 Feb 17.

Department of Endocrinology & Metabolism, Institute of Postgraduate Medical Education and Research/SSKM Hospital, Kolkata, West Bengal, India.

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http://dx.doi.org/10.1136/bcr-2016-214624DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483552PMC
February 2016
8 Reads

Hypertrophic Osteoarthropathy and Follicular Thyroid Cancer: A Rare Paraneoplastic Syndrome.

Eur Thyroid J 2015 Dec 14;4(4):266-70. Epub 2015 Aug 14.

Unité Thyroïde Tumeurs Endocrines, Groupe Hospitalier et Faculté de Médecine Pitié-Salpêtrière, Institut du Cancer, Université Pierre et Marie Curie, Paris, France.

Background: Hypertrophic osteoarthropathy (HOA) is a rare condition characterized by bone and joint pain and digital clubbing usually associated with bronchopulmonary diseases. Primary HOA is rare and the pathogenesis remains unclear.

Objectives: Cases of HOA as a paraneoplastic syndrome associated with thyroid carcinoma are very rare - only 2 cases have been described in the literature. Read More

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http://dx.doi.org/10.1159/000437052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716416PMC
December 2015
39 Reads

Pachydermoperiostosis.

Indian J Dermatol Venereol Leprol 2016 Jan-Feb;82(1):57-8

Department of Dermatology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.

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http://dx.doi.org/10.4103/0378-6323.172901DOI Listing
October 2016
8 Reads

Hypertrophic Osteoarthropathy.

J Am Osteopath Assoc 2015 Dec;115(12):745

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http://dx.doi.org/10.7556/jaoa.2015.153DOI Listing
December 2015
6 Reads

[If digital clubbing appears bear Marie-Bamberger disease in mind].

Z Rheumatol 2015 Oct;74(8):728-30

Klinik für Rheumatologie, HELIOS Seehospital Sahlenburg, Nordheimstr. 201, 27476, Cuxhaven, Deutschland.

Secondary hypertrophic osteoarthropathy, also known as Marie-Bamberger disease, occurs in up to 5 % of patients with non-small cell lung cancer (NSCLC). If the syndrome constellation of finger clubbing and bone pain on palpation is recognized early, lung cancer can be diagnosed at an early stage. This article reports the case of a 52-year-old male patient with knee pain, distal edema, watchglass nails and finger clubbing which first appeared in August 2013. Read More

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http://dx.doi.org/10.1007/s00393-015-1662-6DOI Listing
October 2015
29 Reads

Aortopulmonary window and interrupted aortic arch with Eisenmenger syndrome in an adult.

Circulation 2015 Sep;132(13):e157-9

From Departments of Cardiology (S.K.S, D.A., A.S., K.C., M.K.S., K.B.) and Radio-Diagnosis (K.G.), RNT Medical College, Udaipur, India.

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http://dx.doi.org/10.1161/CIRCULATIONAHA.114.014707DOI Listing
September 2015
31 Reads

Hypertrophic Pulmonary Osteoarthropathy in Anaplastic Lymphoma Kinase (ALK)-positive Lung Cancer.

Intern Med 2015 15;54(16):2045-9. Epub 2015 Aug 15.

The First Department of Internal Medicine, Shinshu University School of Medicine, Japan.

A 49-year-old man was admitted to a hospital with chest pain and polyarthralgia. Chest radiography showed abnormal findings, and chest computed tomography showed a mass in the right lung. A transbronchial lung biopsy led to a diagnosis of anaplastic lymphoma kinase (ALK)-positive adenocarcinoma. Read More

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http://dx.doi.org/10.2169/internalmedicine.54.4452DOI Listing
April 2016
2 Reads

Hypertrophic osteoarthropathy presenting as inflammatory arthritis.

Arthritis Rheumatol 2015 Nov;67(11):3036

University Medical Center, Gottingen, Germany.

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http://dx.doi.org/10.1002/art.39272DOI Listing
November 2015
5 Reads

Pachydermoperiostosis and bladder cancer.

Dermatol Online J 2015 Jun 16;21(6). Epub 2015 Jun 16.

San Camillo Hospital, Italy.

Pachydermoperiostosis or the Touraine-Soulente-Golé syndrome is a rare monogenetic disorder characterized by pachydermia, periostosis and digital clubbing accounts for approximately 3∼5% of all patients with hypertrophic osteoarthropathy. Missense mutations in SLCO2A1 and HPGD genes could plausibly underlie the pathogenesis of pachydermoperiostosis. Patients have usually a favorable outcome with very few cases associated with cancer. Read More

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June 2015
15 Reads

[Pachydermoperiostosis].

Rev Prat 2015 Jan;65(1):26-7

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January 2015
5 Reads

Pulmonary epithelioid hemangioendothelioma: Nuclear medicine and 18F-FDG PET/CT findings.

Rev Esp Med Nucl Imagen Mol 2015 Nov-Dec;34(6):393-5. Epub 2015 Mar 21.

Department of Radiology, Mayo Clinic, AZ 85259, USA.

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http://dx.doi.org/10.1016/j.remn.2015.02.004DOI Listing
June 2017
3 Reads

Imaging observations of pulmonary inflammatory myofibroblastic tumors in patients over 40 years old.

Oncol Lett 2015 Apr 2;9(4):1877-1884. Epub 2015 Feb 2.

Department of Medical Imaging, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, Jiangsu 210002, P.R. China.

Pulmonary inflammatory myofibroblastic tumors (PIMTs) are extremely rare in adults. If occurring in patients >40 years old, PIMT should be rapidly distinguished from lung cancer. The present study aimed to characterize the imaging features of PIMT in patients >40 years old in order to improve the diagnosis of PIMT. Read More

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http://dx.doi.org/10.3892/ol.2015.2923DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356430PMC
April 2015
2 Reads

Evaluation of digital clubbing.

Authors:
Chun Wai Chan

Aust Fam Physician 2015 Mar;44(3):113-6

MD MPH DABFM, Lecturer, Department of Family Medicine, International Medical University, Malaysia.

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March 2015
5 Reads

Hypertrophic osteoarthropathy associated with esophageal cancer.

Intern Med 2015 ;54(3):357-8

Division of Rheumatology and Clinical Immunology, Department of Medicine, Jichi Medical University, Japan.

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http://dx.doi.org/10.2169/internalmedicine.54.3458DOI Listing
June 2015
4 Reads

Hypertrophic Pulmonary Osteoarthropathy: A Rare But Treatable Condition in Palliative Medicine.

J Pain Symptom Manage 2015 Aug 17;50(2):263-7. Epub 2015 Feb 17.

Wellmont Cancer Institute, Wellmont Health System, Kingsport, Tennessee, USA.

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http://dx.doi.org/10.1016/j.jpainsymman.2015.02.005DOI Listing
August 2015
9 Reads

Joint pain in a man with lung cancer.

Cleve Clin J Med 2015 Jan;82(1):18-9

Academic Hospitalist, Good Shepherd Medical Center, Longview, TX.

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http://dx.doi.org/10.3949/ccjm.82a.13137DOI Listing
January 2015
8 Reads

Hypertrophic pulmonary osteoarthropathy in a patient with lung cancer.

Intern Med 2014 1;53(23):2757-8. Epub 2014 Dec 1.

Department of Radiology, Kaohsiung Veterans General Hospital, Taiwan.

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http://pdfs.journals.lww.com/jto/2010/07000/Hypertrophic_Pul
Web Search
May 2015
4 Reads
0.970 Impact Factor

[Agenesis of the pulmonary valve: report of a case in a 24-year old Senegalese woman].

Pan Afr Med J 2014 24;18:76. Epub 2014 May 24.

UFR des sciences de la santé de l'université de Thiès. BP 43 Thiès, Senegal ; Hôpital Général Grand Yoff Dakar, Senegal.

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http://dx.doi.org/10.11604/pamj.2014.18.76.3250DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231241PMC
July 2015
11 Reads

A rare case of congenital complex pulmonary AV fistula.

BMJ Case Rep 2014 Oct 17;2014. Epub 2014 Oct 17.

Department of Cardiology, King George's Medical University, Lucknow, Uttar Pradesh, India.

A 15-year-old boy presented with central cyanosis with clubbing and dyspnoea on exertion. Cardiovascular examination did not reveal any abnormality. ECG was normal. Read More

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http://dx.doi.org/10.1136/bcr-2014-205939DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202061PMC
October 2014
5 Reads

Non-traumatic calcifications/ossifications of the bone surface and soft tissues of the wrist, hand and fingers: a diagnostic approach.

Diagn Interv Imaging 2014 Nov 16;95(11):1035-44. Epub 2014 Sep 16.

Radiologie ostéo-articulaire, hôpital Lariboisière, AP-HP, 2, rue Ambroise-Paré, 75475 Paris cedex 10, France.

In the absence of obvious trauma, the calcifications/ossifications of the bone surface and soft tissues of the wrist, hand and fingers can be challenging and may not be noticed or lead to unnecessary examinations and monitoring. Although these are usually benign conditions and despite a favorable spontaneous outcome, surgical resection may be required and recurrence may occur. In practice, only paraneoplastic syndromes such as secondary hypertrophic osteoarthropathy (Pierre Marie-Bamberger syndrome) may reveal a malignant tumor, most often pulmonary. Read More

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http://dx.doi.org/10.1016/j.diii.2014.07.004DOI Listing
November 2014
11 Reads

Giant single atrium.

Int J Cardiol 2014 Nov 7;177(1):e37-8. Epub 2014 Aug 7.

St. Raphael of St. Francis - Nsambya Hospital, Kampala, Uganda.

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https://linkinghub.elsevier.com/retrieve/pii/S01675273140150
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http://dx.doi.org/10.1016/j.ijcard.2014.07.276DOI Listing
November 2014
10 Reads

Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up.

Rheumatol Int 2014 Nov 12;34(11):1539-44. Epub 2014 May 12.

Department of Pediatric Genetics, Cerrahpaşa Medical School, Istanbul University, Istanbul, Turkey,

Autosomal recessive primary hypertrophic osteoarthropathy1 (PHOAR1) is characterized by delayed closure of the fontanels, digital clubbing, arthropathy and periostosis. Homozygous mutations in hydroxyprostaglandin dehydrogenase (HPGD) gene are the underlying pathology of PHOAR1. The aim of this study was to analyze the HPGD gene and the changing clinical and radiological findings with advancing age of two siblings with the diagnosis of PHOAR1. Read More

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http://dx.doi.org/10.1007/s00296-014-3037-8DOI Listing
November 2014
28 Reads

Improved severe hepatopulmonary syndrome after liver transplantation in an adolescent with end-stage liver disease secondary to biliary atresia.

Clin Mol Hepatol 2014 Mar 26;20(1):76-80. Epub 2014 Mar 26.

Department of Surgery, Keimyung University School of Medicine, Daegu, Korea.

Hepatopulmonary syndrome (HPS) is a serious complication of end-stage liver disease, which is characterized by hypoxia, intrapulmonary vascular dilatation, and liver cirrhosis. Liver transplantation (LT) is the only curative treatment modality for patients with HPS. However, morbidity and mortality after LT, especially in cases of severe HPS, remain high. Read More

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http://dx.doi.org/10.3350/cmh.2014.20.1.76DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992334PMC
March 2014
3 Reads

Differential cyanosis and clubbing sparing a single limb.

J Am Coll Cardiol 2014 Apr 19;63(14):e33. Epub 2014 Feb 19.

Department of Cardiology, Seth G. S. Medical College and The King Edward VII Memorial Hospital, Mumbai, India.

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https://linkinghub.elsevier.com/retrieve/pii/S07351097140044
Publisher Site
http://dx.doi.org/10.1016/j.jacc.2013.11.058DOI Listing
April 2014
11 Reads