Cystic disease with sparing of lung bases

Die zystische Degeneration der Adventitia (ZAD) in der A.iliaca externa ist mit zehn in der Literatur beschriebenen Fällen ein seltenes Phänomen. Eine rasch auftretende, einseitige Ischämiesymptomatik bei jungen Patienten sollte daran denken lassen und eine erweiterte präoperative Abklärung zur Folge haben. Die klassische Therapie mit Gefässresektion und Veneninterponat wird seit jeher kontrovers diskutiert. Wir berichten über einen Fall mit rezidivfreiem Verlauf über drei Jahre nach Exarterektomie.

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CYSTIC DISEASE OF THE LUNGS

The Medical Journal of Australia ◽

10.5694/j.1326-5377.1953.tb84851.x ◽

1953 ◽

Vol 1 (21) ◽

pp. 732-736

Author(s):

C. G. Bayliss

Keyword(s):

Cystic Disease

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Cherubism: Report of a Case

Journal of Health and Allied Sciences NU ◽

10.1055/s-0040-1722425 ◽

2020 ◽

Author(s):

Sachin G. Ram ◽

Vidya Ajila ◽

Subhas G. Babu ◽

Pushparaja Shetty ◽

Shruthi Hegde ◽

...

Keyword(s):

Fibrous Dysplasia ◽

Developmental Disorder ◽

Present Report ◽

Maximum Growth ◽

Posterior Region ◽

Therapeutic Management ◽

Age Group ◽

Cystic Disease ◽

Radiographic Features

AbstractCherubism, also known as familial fibrous dysplasia of the jaws or familial multilocular cystic disease is a rare hereditary, developmental disorder. This condition affects the posterior region of the jaws bilaterally in children belonging to the age group of 2 to 5 years. Maximum growth is recorded till puberty after which the lesion regresses over a period of time. Cherubism classically manifests radiographically as bilateral, multilocular radiolucencies affecting the posterior mandible and maxilla. Therapeutic management varies from patient to patient and is directed mainly by esthetic and functional concerns. The present report highlights the clinical and radiographic features of nonfamilial cherubism in a 6-year-old girl.

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Educational Case: Pancreatic Cystic Disease: A Multimodal Diagnostic Approach to Determine Clinical Management

Academic Pathology ◽

10.1177/2374289521998031 ◽

2021 ◽

Vol 8 ◽

pp. 237428952199803

Author(s):

Daniel Geisler ◽

Samer N. Khader

Keyword(s):

Medical Education ◽

Clinical Management ◽

Organ System ◽

Learning Objectives ◽

National Standards ◽

Cystic Disease ◽

Full List ◽

Additional Information ◽

Disease Mechanisms ◽

Basic Competencies

The following fictional case is intended as a learning tool within the Pathology Competencies for Medical Education (PCME), a set of national standards for teaching pathology. These are divided into three basic competencies: Disease Mechanisms and Processes, Organ System Pathology, and Diagnostic Medicine and Therapeutic Pathology. For additional information, and a full list of learning objectives for all three competencies, see http://journals.sagepub.com/doi/10.1177/2374289517715040 . 1

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CONGENITAL CYSTIC DISEASE OF LUNG ASSOCIATED WITH ANOMALOUS ARTERIES

Journal of Thoracic Surgery ◽

10.1016/s0096-5588(20)31219-8 ◽

1952 ◽

Vol 23 (1) ◽

pp. 55-65 ◽

Cited By ~ 2

Author(s):

Frederick G. Kergin

Keyword(s):

Cystic Disease

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Is it always Wilms’ tumor? Localized cystic disease of the kidney in an infant. An extremely rare case report and review of the literature

Pediatric Reports ◽

10.4081/pr.2020.8483 ◽

2020 ◽

Vol 12 (1) ◽

Author(s):

Christos Kaselas ◽

Charikleia Demiri ◽

Vasilios Mouravas ◽

Eleni Koutra ◽

Kleanthis Anastasiadis ◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Wilms Tumor ◽

Pediatric Population ◽

Benign Disease ◽

Cystic Disease ◽

Proper Treatment ◽

Review Of The Literature ◽

Rare Case Report ◽

Renal Malignancies

Localized Cystic Disease of the Kidney (LCDK) is an extremely rare benign disease in pediatric population. Although its management is conservative and generally requires no treatment, the unfamiliarity with the disease can expose such patients to misdiagnosis as renal malignancies or uncertainty for proper treatment. We report such a case in an infant and review the current literature.

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