scholarly journals A Patient with Intralobar Pulmonary Sequestration: A Rare Congenital Anomaly

2012 ◽  
Vol 20 (1) ◽  
pp. 99-102 ◽  
Author(s):  
Walter Beneduzzi Fiorotto ◽  
Leandro Zacarias ◽  
Marcio Ricardo dos Santos ◽  
Flavio Borges de Oliveira ◽  
Jamil Elias Dib Filho ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Rare Congenital Anomaly ◽  
Intralobar Pulmonary Sequestration

The rare congenital anomaly of pulmonary sequestration experience and review of literature

2010 ◽  
Vol 26 (4) ◽  
pp. 251-254 ◽  
Author(s):  
Atilla Pekçolaklar ◽  
Necati Çitak ◽  
Muzaffer Metin ◽  
Abdülaziz Kök ◽  
Alper Çelikten ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Review Of Literature ◽  
Rare Congenital Anomaly

Use of Amplatzer Vascular Plugs for the treatment of combined extralobar and intralobar pulmonary sequestration in a 5-year-old child

2016 ◽  
Vol 26 (7) ◽  
pp. 1441-1444 ◽  
Author(s):  
Carrie E. Herbert ◽  
Surendranath R. Veeram Reddy ◽  
Matthew S. Lemler
Keyword(s):  
Heart Failure ◽  
Respiratory Symptoms ◽  
Pulmonary Sequestration ◽  
Normal Lung ◽  
Visceral Pleura ◽  
Recurrent Infections ◽  
Rare Congenital Anomaly ◽  
Extralobar Pulmonary Sequestration ◽  
Intralobar Pulmonary Sequestration ◽  
Transcatheter Embolisation

AbstractPulmonary sequestration is a rare congenital anomaly that can be asymptomatic or present with recurrent infections, respiratory symptoms, or rarely heart failure. Sequestration is classified as intralobar or extralobar on the basis of whether there is separation from normal lung tissue by its own visceral pleura. Classically, patients are treated with surgical resection. We present a case of multivessel, combined intralobar and extralobar pulmonary sequestration treated with transcatheter embolisation.

Retroperitoneal Pulmonary Sequestration: A Rare Congenital Anomaly in a 71-Year-Old Man

1994 ◽  
Vol 152 (6 Part 2) ◽  
pp. 2341-2343 ◽  
Author(s):  
Joel B. Nelson ◽  
Michael D. Blum ◽  
William A. Cook
Keyword(s):  
Congenital Anomaly ◽  
Pulmonary Sequestration ◽  
Rare Congenital Anomaly

scholarly journals Computed Tomography findings of atypical intralobar pulmonary sequestration: Research Article

2021 ◽  
Vol 9 (1) ◽  
pp. 10-10
Author(s):  
Sercan Özkaçmaz ◽  
Muhammed Bilal Akıncı ◽  
Mesut Özgökçe ◽  
İlyas Dündar ◽  
Fatma Durmaz ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Pulmonary Sequestration ◽  
Venous Drainage ◽  
Rare Congenital Anomaly ◽  
Pulmonary Lesions ◽  
Intralobar Sequestration ◽  
Research Article ◽  
Atypical Features ◽  
Intralobar Pulmonary Sequestration ◽  
Different Types

Backgrounds: Bronchopulmonary sequestration (BPS) is a rare congenital anomaly of the lung that has two different types as intralobar and extralobar. In this study, we aimed to present six cases of intralobar sequestration with atypical findings in terms of feeding, drainage and, localization. Methods: Patients diagnosed with intralobar pulmonary sequestration in our clinic between 2015-2019 were evaluated retrospectively. Demographical features and atypical Computed Tomography (CT) findings of the patients were presented by literature. Results: Among 45 patients with intralobar sequestration, six ones (13.3%) (5 males and 1 female) with a mean age of 43.5±25.4 (0-78) years old) had atypical pulmonary findings on CT images. Atypical features regarding arterial supply was detected in 8.9%, venous drainage in 2.2%, location in 4.4%, radiological appearance ın 4.4% and co-existing lesion in 2.2% of the patient with intralobar sequestration. Conclusion: Typical and atypical features of pulmonary sequestration must be well-known for differential diagnosis of solid or cystic pulmonary lesions.

scholarly journals Cor triatriatum dexter, a very rare congenital anomaly presented in a complex pathological context – case presentation

2014 ◽  
Vol 60 (4) ◽  
pp. 160-162
Author(s):  
Liliana Gozar ◽  
Cristina Blesneac ◽  
Rodica Toganel
Keyword(s):  
Congenital Anomaly ◽  
Cytomegalovirus Infection ◽  
Cor Triatriatum ◽  
Anatomical Feature ◽  
Renal Anomalies ◽  
Anatomical Variant ◽  
Case Presentation ◽  
Congenital Cytomegalovirus ◽  
Rare Congenital Anomaly ◽  
Cor Triatriatum Dexter

Abstract Background Cor triatriatum dexter is an extremely rare congenital anomaly, and in most cases, without hemodynamic significance. Congenital cytomegalovirus infection is the most common viral infection, the majority of infected infants being asymptomatic and only 5-15% being symptomatic in the neonatal period. Case report We present the case of a female infant, aged 3 months. Clinical examination reveals cranial and facial anomalies. The karyotype was normal. Laboratory tests revealed the presence of anti-CMV antibodies in urine. Imaging studies showed cerebral and renal anomalies. Echocardiographic exam revealed a congenital anatomical feature without hemodynamic significance - cor triatriatum dexter. Conclusions although cytomegalovirus infection is mostly asymptomatic, it can present as a complex pathological association, in which a congenital cardiac anatomical feature without hemodynamic significance, considered by some authors as an anatomical variant, can appear

scholarly journals Roberts uterus: a rare congenital anomaly

2017 ◽  
Vol 6 (12) ◽  
pp. 5657
Author(s):  
Nagendra Sardeshpande ◽  
Pratima Chipalkatti ◽  
Jainesh Doctor
Keyword(s):  
Congenital Anomaly ◽  
Abdominal Pain ◽  
Adnexal Mass ◽  
Lower Abdominal Pain ◽  
Uterine Horn ◽  
Transabdominal Ultrasound ◽  
Septate Uterus ◽  
Bicornuate Uterus ◽  
Rare Congenital Anomaly ◽  
Hysteroscopic Resection

A 23-year-old girl presented with severe cyclical lower abdominal pain during menstruation since menarche, which had increased since the last 4 years. Transabdominal ultrasound showed adnexal mass with no internal vascularity; MRI reported it as bicornuate uterus with one non-communicating right uterine horn with haematometra. On hysteroscopy there was evidence of septate uterus communicating only to the left ostia. Ultrasonography-guided hysteroscopic resection of septa with drainage of haematometra was done. Patient is presently asymptomatic.

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