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Thematische Bibliographien / Adrenal pseudocyst

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Zeitschriftenartikel

Auswahl der wissenschaftlichen Literatur zum Thema „Adrenal pseudocyst“

Autor: Grafiati

Veröffentlicht am 7. Juni 2025

Zuletzt aktualisiert am 2. August 2025

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Zeitschriftenartikel zum Thema "Adrenal pseudocyst"

1

Shanthi, Vissa, Shyam Sundar Rao Byna, and Mohan Rao Nandam. "Giant Adrenal Pseudocyst- A Case Report." International Journal of Research and Review 6, no. 1 (2019): 83–85. https://doi.org/10.5281/zenodo.3984765.

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Adrenal pseudocysts are uncommon lesions which are asymptomatic and have an estimated incidence of 0.064% to 0.18%.Cystic lesions of adrenal may vary from cystic malignant neoplasms to pseudocysts. Adrenal pseudocysts are asymptomatic and are discovered incidentally during radiography or at autopsy. They lack lining epithelium and are surrounded by fibrous tissue. Though the adrenal pseudo cysts have characteristic radiographic appearance, it is difficult to distinguish it from cystic neoplasm of adrenal. We report a case pseudocyst of left adrenal in 30 years female presenting with left lumba

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2

Larabee, Shannon M., Jason S. Radowsky, Guangjing Zhu, John Papadimitriou, and Deborah Stein. "Giant adrenal pseudocyst in trauma patient." Trauma 22, no. 2 (2019): 155–58. http://dx.doi.org/10.1177/1460408619881540.

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Adrenal pseudocysts are a subclass of adrenal cysts frequently found as incidentalomas. Here, we present the case of a 67-year-old man with an adrenal pseudocyst suspicious for hemorrhage after a fall who was urgently transferred to a tertiary care trauma center for care.

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3

Oussama, JADDI, Rafi Sana, Ijdda Sara, El Mghari Ghizlane, and EL Ansari Nawal. "Adrenal Pseudocyst: Rare Clinical Presentation and Review of the Literature." International Journal of Clinical Science and Medical Research 05, no. 05 (2025): 114–17. https://doi.org/10.5281/zenodo.15373548.

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Abstract Adrenal pseudocysts are rare, non-neoplastic lesions of the adrenal gland, often discovered incidentally during imaging for unrelated reasons. Representing 32–80% of adrenal cysts, they are characterized histologically by a fibrous wall lacking epithelial or endothelial lining. Their etiology is uncertain but frequently linked to intra-adrenal hemorrhage, trauma, or degenerative changes. Most pseudocysts are asymptomatic, but large lesions may cause compressive symptoms or complications such as hemorrhage or rupture. This article presents the case of a 36-year-old woman with rig

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4

Habra, Mouhammed Amir, Barry W. Feig, and Steven G. Waguespack. "Adrenal Pseudocyst." Journal of Clinical Endocrinology & Metabolism 90, no. 5 (2005): 3067–68. http://dx.doi.org/10.1210/jc.2004-2538.

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5

Alaswad, Faris. "Adrenal Pseudocyst, Case Report." Journal of Clinical Surgery and Research 5, no. 4 (2024): 01–05. http://dx.doi.org/10.31579/2768-2757/126.

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Pseudocyst type of adrenal cysts is most common; however, this type of ectopic cyst is quite rare in excessively large adrenal cysts. A35-year-old woman was admitted to our institution with distension of her right flank and the upper quadrant of her abdomen. Abdominal ultrasonography revealed a cystic lesion with a homogenous anechoic texture, and measuring 28 cm in diameter. Computed tomography imaging displayed a giant cystic lesion adjacent to the liver, pancreas, kidney. The origin of the cyst was not identified. We were not able to make a preoperative diagnosis; therefore, the patient und

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6

White, Christopher M., Harvey Greenberg, and Brian R. Davis. "Giant Hemorrhagic Adrenal Pseudocyst in Pregnancy." Donald School Journal of Ultrasound in Obstetrics and Gynecology 8, no. 1 (2014): 105–8. http://dx.doi.org/10.5005/jp-journals-10009-1344.

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ABSTRACT Adrenal cysts are a rare diagnosis, particularly in pregnancy. We report the case of a 32-year-old pregnant woman with an adrenal pseudocyst in her 28th week of pregnancy. This represents the 13th case of an adrenal pseudocyst in pregnancy reported in the literature. The patient presented to our facility complaining of abdominal pain, believing she could be in preterm labor. After further evaluation and surgery, she was diagnosed with a left adrenal pseudocyst. In this report, we will not only describe our case but also discuss the relevance of the findings to what is already present

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7

Sezhian, N., D. Rimal, and G. Suresh. "Adrenal Pseudocyst-Diagnostic Dilemma." Scottish Medical Journal 50, no. 2 (2005): 81. http://dx.doi.org/10.1177/003693300505000214.

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8

Bartlett, David L., Arnold Cohen, Ruby Huttner, and Michael H. Torosian. "Adrenal pseudocyst in pregnancy." Surgery 118, no. 3 (1995): 567–70. http://dx.doi.org/10.1016/s0039-6060(05)80375-7.

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9

Halefoglu, Ahmet Mesrur, Alkin Ercan, Ahmet Yasar, and Elife Sahan. "Giant adrenal hemorrhagic pseudocyst." European Journal of Radiology Extra 63, no. 1 (2007): 35–37. http://dx.doi.org/10.1016/j.ejrex.2007.04.005.

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10

Schrank, Yolanda, and Miguel Madeira. "Massive: Hemorrhagic Adrenal Pseudocyst." American Journal of Medicine 127, no. 9 (2014): 823–25. http://dx.doi.org/10.1016/j.amjmed.2014.04.021.

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