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Loculated neonatal chylothorax treated with octreotide: complete recovery while on unrestricted full fat breast milk.

Authors:
Charles C Roehr Andreas Jung Oliver A Curcin Hans Proquitte Hannes Hammer Roland R Wauer

Ann Thorac Surg 2005 Nov;80(5):1981-2; author reply 1982

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http://dx.doi.org/10.1016/j.athoracsur.2005.01.040DOI Listing
November 2005

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[Management of chylous ascites and chylothorax. Report of one case].

Authors:
Paulina Jofré Bruno Grassi Carlos Benítez

Rev Med Chil 2020 Aug;148(8):1202-1206

Departamento de Gastroenterología, Pontificia Universidad Católica de Chile, Santiago, Chile.

Chylous Ascites (CA) and chylothorax (CTx) are associated with obstruction, disruption or insufficiency of the lymphatic system. We report a 68-year-old male, with a history of alcoholic cirrhosis, who had recurrent events of CTx and CA. After a complete study, no other etiologies other than portal hypertension were found. Read More

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68Ga-DOTATOC-PET/CT-guided resection of a primary intraosseous meningioma: technical note.

Authors:
Gerardo Y Guinto-Nishimura Juan L Gómez-Amador Nora Kerik-Rotenberg Rodrigo Uribe-Pacheco Marcos V Sangrador-Deitos José J Martínez-Manrique

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1Neurosurgery Department and.

Primary intraosseous meningiomas (PIMs) are rare tumors that present with a variable radiological appearance and a clinical behavior that is considerably different from that of intracranial meningiomas. Treatment of PIMs consists of complete resection, which may be difficult to achieve due to the lack of clear tumor margins on conventional imaging studies. PET/CT using 68Ga-DOTA-conjugated peptides has been used for the diagnosis and treatment planning of different types of meningiomas due to these tracers' affinity to somatostatin receptors, which are found in most meningiomas. Read More

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[The use of long-acting somatostatin analogs in congenital hyperinsulinism].

Authors:
E E Novokreshhennyx D N Gubaeva M A Melikyan

Probl Endokrinol (Mosk) 2020 Oct 24;66(5):70-78. Epub 2020 Oct 24.

Endocrinology research Centre.

Background: Children with congenital hyperinsulinism (CHI), a severe orphan disease, are still one of the most demanding patients in the endocrinology practice. The use of first- and second-line drugs is not always effective and has a number of restrictions. Lanreotide - long-acting somatostatin - represents an alternative insulinostatic therapy. Read More

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October 2020
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[Epidemiology, clinical manifestations and efficiency of different methods of treatment of acromegaly according to the United Russian Registry of Patients with Pituitary Tumors].

Authors:
Zhanna E Belaya Olga O Golounina Liudmila Y Rozhinskaya Galina A Melnichenko Michail А Isakov Alexander S Lutsenko Tatiana Alekseeva Tatiana S Zenkova Elena G Przhiyalkovskaya Galina M Panyushkina Olga B Ilukhina Elena I Ivanova Ekaterina A Krishtal Alla A Vachygova Ekaterina A Pigarova Larisa K Dzeranova Evgenia I Marova Svetlana D Arapova Elizaveta O Mamedova Tatiana A Grebennikova Mikhail B Antsiferov Alexander V Dreval Ivan I Dedov

Probl Endokrinol (Mosk) 2020 Aug 4;66(1):93-103. Epub 2020 Aug 4.

Endocrinology Research Centre.

Background: The registry is the main source of information about patients with acromegaly for assessing the quality of medical care, effectiveness of treatment, determining the compliance of real clinical practice with existing standards and patient management protocols.

Aims: To evaluate epidemiological, demographic and clinical characteristics of acromegaly in Russian Federation and effectiveness of treatment modalities.

Materials And Methods: The object of the study was the database of the united Russian registry of patients with pituitary tumors with specific analysis of patients with acromegaly only. Read More

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August 2020
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Chylothorax Associated with Congenital Complete Atrioventricular Block.

Authors:
Shuhei Fujino Hidehiko Maruyama Keiko Tsukamoto Hiroshi Ono Tetsuya Isayama Yushi Ito

AJP Rep 2020 Oct 3;10(4):e403-e407. Epub 2020 Dec 3.

Division of Neonatology, Center for Maternal-Fetal, Neonatal and Reproductive Medicine, National Center for Child Health and Development, Tokyo, Japan.

 Congenital complete atrioventricular block (CCAVB) associated with congenital chylothorax is a rare finding that has been reported in only one case in the literature. We report here the case of an infant with CCAVB complicated by congenital chylothorax.  We present the case of a male neonate with a birth weight of 2114 g. Read More

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October 2020
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