Relevant bibliographies by topics / Rare cyst

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Rare cyst'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Rare cyst"

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Daniel, Phillip, Siddharth Shukla, Nidhi Prabhakar, et al. "Infected Pancreatic Hydatid Cyst with Cysto-Pancreatic Fistula Presenting as Acute Pancreatitis." Journal of Digestive Endoscopy 10, no. 04 (2019): 234–36. http://dx.doi.org/10.1055/s-0040-1708069.

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AbstractHydatid cysts can be found in almost any organ of the body with the most common sites being liver, lung, spleen, and kidney. A pancreatic hydatid cyst is rare but an isolated pancreatic hydatid cyst is even rarer. Cysts in the head of pancreas usually present with jaundice, whereas cysts located in the body and tail are usually asymptomatic. We present a rare case of isolated pancreatic hydatid cyst that presented with acute pancreatitis and mimicked a pancreatic fluid collection.
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Dr., A. Verma, S. Jain Dr., M. Jain Dr., and A. Mundra Dr. "Tarlov Cyst: A Case Report." Orthopaedic Journal of M P Chapter 26, no. 1 (2020): 45–48. https://doi.org/10.5281/zenodo.3969847.

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Case Report: Tarlov cyst is rare perineural cyst, which may be symptomatic and present with with low back pain, sciatica, coccydynia or cauda equina syndrome. Symptomatic tarlov cyst needs to be removed surgically. We present such a rare case of symptomatic sacral cystic mass (tarlov cyst) presenting with severe lower back pain for months which was successfully treated by sacral laminotomy and cyst excision. The aim of reporting this case was to create awareness among the surgeons regarding this rare entity and to include it in differential diagnosis of chronic low back pain.
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Patankar, AP, and JH Sheth. "Dermoid cyst: A rare intramedullary inclusion cyst." Asian Journal of Neurosurgery 7, no. 2 (2012): 81. http://dx.doi.org/10.4103/1793-5482.98651.

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Keskin, Hakan. "Parathyroid cyst: A rare benign mediastinal cyst." Turkish Journal of Thoracic and Cardiovascular Surgery 25, no. 4 (2017): 663–66. http://dx.doi.org/10.5606/tgkdc.dergisi.2017.14057.

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Agrawal, Vivek, and Rohit Ranjan. "Paraurethral Cyst: A Rare Case Report." New Indian Journal of Surgery 8, no. 4 (2017): 607–9. http://dx.doi.org/10.21088/nijs.0976.4747.8417.30.

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Daware, Ankit, Jaykumar Gunjkar Aishwarya Khalatkar, and Manav Khalatkar. "Rare Case of Dorsal Epidermoid Cyst." International Journal of Science and Research (IJSR) 12, no. 11 (2023): 1784–86. http://dx.doi.org/10.21275/sr231124013944.

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Bhatia, Ruby, Manjit Kaur Mohi, Anju Gupta, and Sonia Goyal. "Para vaginal dermoid cyst: a rare occurrence." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 2 (2019): 776. http://dx.doi.org/10.18203/2320-1770.ijrcog20190324.

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Dermoid cyst (cystic teratoma) showing well differentiated derivatives of all three germs cell layers is a benign germ cell tumour. Ovaries remain the commonest site. Paravaginal dermoid cyst is a rare occurrence. Pre-operative diagnosis is usually difficult in majority of cases. They constitute less than 4% of all extragonadal teratomas. A 28-year old, P2L2 female presented with paravaginal cyst, 10×10cms, non-tender, soft swelling, cystic in consistency occupying posterior and left part of rectovaginal septum. Trans vaginal excision of cyst under regional anaesthesia done. Cyst was ruptured
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del Olmo Martínez, Lourdes, and Benito Velayos Jiménez. "Rare pancreatic cyst: Lymphangioma." Gastroenterología y Hepatología (English Edition) 44, no. 10 (2021): 726–27. http://dx.doi.org/10.1016/j.gastre.2020.09.009.

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V, Srinivasa, Nahas T K, Sandeepjith P, and Balu K G. "A RARE KLESTADT’S CYST." Journal of Evolution of Medical and Dental Sciences 6, no. 09 (2017): 741–43. http://dx.doi.org/10.14260/jemds/2017/160.

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Kumar, A. Vinay, Renuka Rao, M. Rajender, and A. Raghu Kanth. "Rare Mediastinal Hydatid Cyst." Indian Journal of Chest Diseases and Allied Sciences 57, no. 3 (2022): 187–90. http://dx.doi.org/10.5005/ijcdas-57-3-187.

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Dissertations / Theses on the topic "Rare cyst"

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Bowen, Simon Andrew. "Aspects of the population biology of the cyst nematode parasites of oilseed rape." Thesis, University of Bedfordshire, 1988. http://hdl.handle.net/10547/596742.

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Investigation of the host-parasite relationship between oilseed rape, Heterodera cruciferae and H. schachtii has shown that the rate of hatching, development and reproduction is strongly influenced by temperature, two possible generations occurring on an autumn-sown crop. H.schachtii preferred warmer temperatures, hatched and reproduced more than H. cruciferae. Comparisons between newly-formed eggs in cysts and egg sacs showed that their different hatching responses were related to their physiology; cyst-bound eggs hatched poorly whereas juveniles hatched readily from egg sacs and facilitated
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Moore, Jenna Marie. "Effects of Soybean Seeding Rate on Plant-to-Plant Variability, Yield, and Soybean Cyst Nematode." The Ohio State University, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1618507332113264.

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Silva, Ricardo Augusto Custodio da. "Cultivo de Dendrocephalus brasiliensis (Pesta, 1921) visando à aplicação em aquicultura." Universidade Federal de São Carlos, 2016. https://repositorio.ufscar.br/handle/ufscar/8282.

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Submitted by Daniele Amaral (daniee_ni@hotmail.com) on 2016-10-20T19:44:51Z No. of bitstreams: 1 TeseRACS.pdf: 3547391 bytes, checksum: fe9bc399d15d41ee702720017aabc920 (MD5)<br>Approved for entry into archive by Marina Freitas (marinapf@ufscar.br) on 2016-11-08T18:43:52Z (GMT) No. of bitstreams: 1 TeseRACS.pdf: 3547391 bytes, checksum: fe9bc399d15d41ee702720017aabc920 (MD5)<br>Approved for entry into archive by Marina Freitas (marinapf@ufscar.br) on 2016-11-08T18:44:01Z (GMT) No. of bitstreams: 1 TeseRACS.pdf: 3547391 bytes, checksum: fe9bc399d15d41ee702720017aabc920 (MD5)<br>Made availab
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Saulez, Montague Newton. "An endoscopic and immunopathological study of respiratory tract disorders in thoroughbred racehorses." Thesis, University of Pretoria, 2008. http://hdl.handle.net/2263/25240.

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Much of the impetus for this research can be attributed to Kenneth W. Hinchcliff, who has studied exercise-induced pulmonary haemorrhage (EIPH) extensively. This thesis focused on EIPH in Thoroughbred racehorses competing in South Africa. Using tracheobronchoscopy, the prevalence and severity of EIPH and the association with racing performance was determined. Thereafter, the prevalence of other respiratory tract disorders and their association with racing performance is reported. This is followed by a study assessing interobserver variability using grading systems in the detection of respirato
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EGAN, THOMAS F. "THE FREQUENCY-DEPENDENCE OF THE NMR LONGITUDINAL RELAXATION RATE, T(1)(-1), OF WATER IN CYSTS OF THE BRINE SHRIMP (ARTEMIA)." Thesis, 1986. http://hdl.handle.net/1911/15968.

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The NMR spin-lattice relaxation rate, T(,1)('-1), of water is independent of the Larmor frequency, (omega)/2(pi), in the normal rf range. However, T(,1)('-1) of intracellular water in biological systems, which accounts for as much as 80% of the cell mass, is frequency-dependent. This indicates that the NMR properties of water in the cellular environment are influenced by long-correlation time processes due to the interaction of water with proteins and other macromolecular constituents of the cell. In this research, the relaxation rate T(,1)('-1) of water in the Artemia (brine shrimp) cyst is e
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Books on the topic "Rare cyst"

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Lelivelt, Cilia L. C. Introduction of beet cyst nematode resistance from Sinapis alba L. and Raphanus sativus L. into Brassica napus L. (oil-seed rape) through sexual and somatic hybridization. [s.n.], 1993.

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Buchanan, Ian A., and Gabriel Zada. Rathke’s Cleft Cysts. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0017.

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Cystic lesions involving the sella have a distinct differential diagnosis including Rathke cleft cyst, cystic pituitary adenoma, craniopharyngioma, arachnoid cyst, and epidermoid among other entities. Workup includes not only cranial imaging but also endocrine evaluation for pituitary dysfunction and ophthalmologic evaluation to assess for visual deficits that may not be immediately apparent to the patient at presentation. Rathke cleft cysts are common and may be found in 20% of autopsy specimens. However, symptomatic Rathke cleft cysts are rare, and surgical decisions should be made judicious
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Ong, Albert C. M., and Timothy Ellam. Autosomal dominant polycystic kidney disease. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0307_update_001.

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Autosomal dominant polycystic kidney disease (ADPKD) is responsible for up to 10% of prevalent patients with end-stage renal disease (ESRD). It is characterized by the enlargement of multiple bilateral renal cysts, present in almost all patients by their fifth decade. Loin pain is a common symptom that may be caused by cyst growth, intracyst haemorrhage, nephrolithiasis, or infection. Gross haematuria is also a common feature, but usually settles spontaneously. Excretory impairment develops after extensive cystic change has occurred and progresses to ESRD in half of all affected patients by th
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Bergmann, Carsten, and Klaus Zerres. Autosomal dominant polycystic kidney disease in children and young adults. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0312.

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Many children with autosomal dominant polycystic kidney disease have renal cysts on ultrasound, some are even being diagnosed antenatally, although the statistics on this are not well understood. Most are asymptomatic but hypertension may be more common than generally appreciated, and a minority of patients develop early renal failure. The cause of early presentations is probably often inheritance of a hypomorphic allele on another gene implicated in cyst formation, or in cilia. Extrarenal manifestations of polycystic kidney disease are very rare in childhood.
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Kühn, Wolfgang, and Gerd Walz. The molecular basis of ciliopathies and cyst formation. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0303.

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Abnormalities of the cilium, termed ‘ciliopathies’, are the prime suspect in the pathogenesis of renal cyst formation because the gene products of cystic disease-causing genes localize to them, or near them. However, we only partially understand how cilia maintain the geometry of kidney tubules, and how abnormal cilia lead to renal cysts, and the diverse range of diseases attributed to them. Some non-cystic diseases share pathology of the same structures. Although still incompletely understood, cilia appear to orient cells in response to extracellular cues to maintain the overall geometry of a
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Raper, Daniel M. S., and John A. Jane. Craniopharyngiomas. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0025.

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Craniopharyngiomas (CPs) are rare tumors arising from the developmental Rathke’s pouch and present in a bimodal distribution peaking at 5 to 14 and 50 to 74 years. Symptoms at onset include visual loss, headache, and hypopituitarism. Most tumors contain solid and cystic components, and fluid within the cyst usually contains cholesterol crystals. Histopathology is classified into adamantinomatous (most common in children) and papillary (almost exclusively in adults) subtypes. Magnetic resonance imaging is the definitive diagnostic modality for sellar and suprasellar lesions. In addition to imag
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Bergmann, Carsten, Nadina Ortiz-Brüchle, Valeska Frank, and Klaus Zerres. The child with renal cysts. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0305.

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Renal cysts of different aetiology are a common diagnosis in paediatric nephrology. The classification is usually based on the clinical picture, morphology, and family history. In syndromic forms, additional features have to be evaluated. Most common are cystic dysplastic kidneys with a broad phenotypic spectrum ranging from asymptomatic clinical courses in unilateral cases to severe, lethal manifestations in patients with considerable bilateral involvement. Simple cysts are rare. Polycystic kidneys are usually subdivided according to the mode of inheritance into autosomal recessive and autoso
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Foggensteiner, Lukas, and Philip Beales. Bardet–Biedl syndrome and other ciliopathies. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0314.

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Ciliopathies encompass a genotypically complex and phenotypically variable and overlapping series of disorders that makes the general term ‘ciliopathies’ very useful. The genes behind these conditions encode parts of the machinery of the primary cilium. This is also true of the major cystic kidney disorders autosomal dominant polycystic kidney disease and autosomal recessive polycystic kidney disease, but the ‘long tails’ of other ciliopathies are characterized by variable nephropathy (often without cyst formation), retinopathy, and effects on brain and skeletal development. Not all have subst
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Hwang, Young-Hwan, and York Pei. Autosomal dominant polycystic kidney disease management. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0309_update_001.

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Management of patients with autosomal dominant polycystic kidney disease (ADPKD) currently comprises non-specific measures including promotion of healthy lifestyle, optimization of blood pressure control, and modification of cardiovascular risk factors. A high water intake of 3–4 L per day in patients with glomerular filtration rate greater than 30 mL/min/1.73 m2 may decrease the risk of kidney stones, but its potential benefit in reducing renal cyst growth is presently unproven. Maintenance of a target blood pressure of 130/80 mmHg is recommended by expert clinical guidelines though this is u
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Lam, Diana L., and John R. Scheel. Fat-Containing, Circumscribed Mass(es). Edited by Christoph I. Lee, Constance D. Lehman, and Lawrence W. Bassett. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190270261.003.0020.

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The majority of fat-containing masses are asymptomatic, but can present as painless, soft, mobile masses. A fat-containing mass within the breast is a benign finding, with the exception of the rare liposarcoma. The differential in non-lactating woman includes a lipoma, hamartoma, lymph node, and fat necrosis. Any atypical presentation of a fat-containing mass (such as thick, nodular septation or capsule, large size &gt;10 cm, a mass that is clinically increasing in size) should raise suspicion for a rare fat-containing tumor such as an atypical lipomatous tumor or well-differentiated liposarco
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Book chapters on the topic "Rare cyst"

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Eltorai, Ibrahim M. "Intradural Extramedullary Bronchgenic Cyst." In Rare Diseases and Syndromes of the Spinal Cord. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-45147-3_7.

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Eltorai, Ibrahim M. "Compression Myelopathy Due to an Intramedullary Cyst Containing Ectopic Choroidal Plexus Tissue." In Rare Diseases and Syndromes of the Spinal Cord. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-45147-3_14.

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Revathy, S., Natrajan Suresh, Mary Lilly, and T. Shoba. "Hidradenoma Papiiliferum of Scalp Masquerading as Epidermal Inclusion CYST — A Rare Case at an Unusual Location." In Recent Developments in Microbiology, Biotechnology and Pharmaceutical Sciences. CRC Press, 2025. https://doi.org/10.1201/9781003618140-20.

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Dropkin, V. H. "Concept of Race in Soybean Cyst Nematode." In World Soybean Research Conference III: Proceedings. CRC Press, 2022. http://dx.doi.org/10.1201/9780429267932-91.

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Oo, Aung Myint. "Esophageal Cysts." In Mastering Endo-Laparoscopic and Thoracoscopic Surgery. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-3755-2_36.

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AbstractEsophageal cysts are rare congenital anomalies of gastrointestinal tract first described by Blasius in 1711. In 1881, Roth also described esophageal cysts and there are two categories namely simple epithelial lined cysts and esophageal duplication cysts. Esophageal duplication cysts are embryologic duplication of part of the esophageal mucosa and submucosa without epithelial duplication. The prevalence of esophageal duplication cysts is 0.0122% and accounts for 10–15% of duplication cysts in the gastrointestinal tract. [1] Esophageal cysts and duplications usually do not have communica
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Riggs, Robert D. "Strategies for Race Stabilization in Soybean Cyst Nematode." In World Soybean Research Conference III: Proceedings. CRC Press, 2022. http://dx.doi.org/10.1201/9780429267932-90.

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Mosca, Vinicio, Miquel Kraft Carré, Alejandro Solís-Peña, Kapil Sahnan, Gianluca Pellino, and Eloy Espín-Basany. "Robotic Procedure for Rare Rectal Conditions: GIST and Tailgut Cysts." In Updates in Surgery. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-33020-9_23.

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Fahlbusch, Rudolf, V. Gerganov, and H. Metwali. "Craniopharyngioma and Rathke’s cleft cysts." In Oxford Textbook of Neurological Surgery, edited by Ramez W. Kirollos, Adel Helmy, Simon Thomson, and Peter J. A. Hutchinson. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780198746706.003.0026.

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Both craniopharyngiomas and Rathke’s cysts are rare pituitary lesions of dysembryogenic origin. Their radiological differentiation may be sometimes difficult due to their occasionally similar imaging characteristics. The surgical management of these lesions, especially of craniopharyngiomas, may be very challenging. Gross total removal of a craniopharyngioma is associated with longer recurrence-free survival but could be associated with higher rate of surgery-related morbidities and pituitary insufficiency. Craniopharyngiomas are considered in the majority of cases to be a ‘chronic disease’. A
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Rosenow, Edward C. "Pericardial Cyst." In Mayo Clinic Challenging Images for Pulmonary Board Review. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199756926.003.0071.

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• Patient had clubbing; thus, mycobacterial infection is less likely • Small-cell cancers almost never cavitate • ↑ incidence of clubbing in cavitated carcinomas. Clubbing with small-cell cancer is rare • See slides 703–714 • Patient was treated for 〉1 year for ...
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Rosenow, Edward C. "Bronchogenic Cyst." In Mayo Clinic Challenging Images for Pulmonary Board Review. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199756926.003.0070.

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• Lesion is not a diaphragmatic hernia: not central, no air-fluid level • Patient had clubbing; thus, mycobacterial infection is less likely • Small-cell cancers almost never cavitate • ↑ incidence of clubbing in cavitated carcinomas. Clubbing with small-cell cancer is rare...
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Conference papers on the topic "Rare cyst"

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Gunterus, Evans, and Alamanda Monik. "Tornwaldt Cyst: Rare Benign Neoplasm Mimicking Nasopharyngeal Carcinoma." In 2nd Global Health and Innovation in conjunction with 6th ORL Head and Neck Oncology Conference (ORLHN 2021). Atlantis Press, 2021. http://dx.doi.org/10.2991/ahsr.k.220206.046.

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Sahni, Sidharth, Joseph Fares, Natty Jumreornvong, Arpun Shah, and Mariam Zakhary. "Dorsal Wrist Impingement Syndrome Pain After Ganglion Cyst Removal – A Case Report." In 27th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2023. https://doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.149_2023.

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A ganglion cyst is a benign fluid-filled sac that develops idiopathically on the dorsal aspect of the wrist by the joint capsule or tendon sheath. It is diagnosed clinically, with MRI and ultrasound used for confirmation. Treatment includes immobilization, aspiration, hydrossection, steroid or hyaluronidase injection, and surgery. Although uncommon, Dorsal Ganglion Cysts (DGC) can lead to Dorsal Wrist Impingement (DWI) syndrome. This syndrome is caused by a thickening of the wrist capsule from overuse, injury, or repetitive procedures. This thickness leads to capsule pinching commonly by the e
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Hena, Kausar, Manchanda Rahul, Lekhi Anshika, Chitra C. H. Sravani, and Jain Nidhi. "Granulosa cell tumour of ovary in a benign looking adnexal mass: A rare occurrence and its management." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685402.

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Granulosa cell tumours are sex cord stromal tumours of the ovary which accounts for 1-2% of all ovarian malignancies. We present a case of a 22 yrs old unmarried girl with chief complaints of dysmenorrhoea for last 4 months. There were no other symptoms and her general physical examination revealed no abnormality. Ultrasonography showed a simple ovarian cyst of 7 x 8 cm in right adnexa with normal Doppler flow and no ascites. Her tumour markers were negative. Per-operative uterus and left sided ovary and upper abdomen was normal. Right ovary showed a simple unilocular cyst of around 8 x 8 cm a
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Torres, J., D. Habib, M. Monk, C. Encarnacion, and S. Alim. "A Rare Case of Infected Bronchogenic Cyst Growing Salmonella Enterica." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a2097.

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Cordeiro, Júlia Coutinho, and José Gilberto de Brito Henriques. "Hemifacial spasm caused by posterior fossa arachnoid cyst: Case Report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.134.

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Context: Hemifacial spasm (HFS) is characterized by continuous or intermittent spasmodic movements at the facial nerve motor territory.1,2,3 It mainly affects middle- aged adults and usually occurs by compression of the facial nerve by anomalous vascular loops of the anteroinferior and vertebral cerebellar artery.2,3,4,5 The arachnoid cyst at the cerebellopontine angle (CPA) is an rare cause of HFS, especially in children. Case report: A six-year-old female patient started presenting at 18 months HFS on the right side. She was initially treated with anticonvulsant without improvement. The pati
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Jost, Carolina Meller, and Robledo Meller Alievi. "Carcinoma of the thyroglossal duct cyst: Case report." In V Seven International Multidisciplinary Congress. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenvmulti2024-001.

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Introduction: Although thyroglossal duct cyst carcinoma is a pathology that is relatively easy to treat, it is an uncommon finding and little reported in the literature. Objective: To report the history, evolution and management of a patient with a thyroglossal duct cyst that progressed to carcinoma, review the pathophysiological nature of the disease, and the scarce literature that addresses this topic. Case summary: Woman, 40 years old, diagnosed in 2018 with a cyst in the thyroglossal duct. He is looking for a Head and Neck surgeon in 2020 to evaluate the case, to whom he reports an increas
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Earasi, K., C. Welch, A. M. Zelickson, et al. "Proteus Empyema as a Rare Complication from an Infected Renal Cyst." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a7200.

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Naing, Su Htet Htet, Sidish Venkataraman, Stephen Tatter, Adrian Laxton, and Mustafa Siddiqui. "Cyst Formation following DBS Electrode Placement: A Rare Complication (P5-11.011)." In 2023 Annual Meeting Abstracts. Lippincott Williams & Wilkins, 2023. http://dx.doi.org/10.1212/wnl.0000000000202723.

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Bhan, N., and D. A. Gross. "A Unique Presentation of a Rare Mediastinal Cyst as a Bilothorax." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a4836.

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Chithra, Sravani, Rahul Manchanda, Hena Kausar, Nidhi Jain, and Anshika lekhi. "Dermoid cyst in an 82-year-old woman: Can be non malignant: Its management." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685399.

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Dermoid cyst of ovary is the second most common type of ovarian germ cell tumor which constitutes 30 to 40% among ovarian tumors. It occurs mostly in women of reproductive age group between 20 and 40 years and very rarely in postmenopausal women. Postmenopause has its own set of symptoms and risks. One such risk is the possibility of malignancy of ovarian cyst with an incidence of 0.5 to 2%. We present an unusual and rare case of an 82 year old woman, who presented with complaints of pain abdomen and constipation for one year duration. Colonoscopy revealed diverticulitis. Despite being treated
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Reports on the topic "Rare cyst"

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Agarwal, Dr Ashna Ashish, and Dr Seema Goel. A RARE CASE OF ISOLATED HYDATID CYST IN SPLEEN. World Wide Journals, 2023. http://dx.doi.org/10.36106/ijar/0906217.

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INTRODUCTION: Hydatid Cyst is a zoonotic infection caused by the larval form of parasite tapeworm Ecchinococcus granulosus. It is most commonly found in liver and rarely found in the spleen. It presents with vague symptoms and usually grows slowly. In this report we describe a rare advanced presentation of a splenic echinococcosis mimicking malignancy. CASE REPORT: A 16yr old female patient presenting with complaints of pain in left lumbar region since three months. Preliminary examination showed splenomegaly with tenderness. Abdominal CT scan showed evidence of well dened, round peripherally
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2

Jangir, Hemlata, Aparna Ningombam, Arulselvi Subramanian, and Subodh Kumar. Traumatic Jejunal Mesenteric Pseudocyst in the Vicinity of Blunt Abdominal Trauma with a Brief Review of Literature. Science Repository, 2023. http://dx.doi.org/10.31487/j.ajscr.2022.04.04.

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Mesenteric pseudocyst (MP) is a rare heterogeneous group of intra-abdominal benign cystic lesions with different etiopathogenesis and clinically silent behaviours. These lesions are introduced as one of the entities based on the histological features of thick fibrous cyst walls, barren of the epithelial lining. Often, they present as expanding abdominal masses or are diagnosed incidentally in conventional radiological studies, exploratory laparotomies, or with symptoms of complications such as infection, torsion, or rupture. Surgical removal of the cyst, with or without resection of the affect
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3

A. Hadad, Majd, Mohammad S. Mallick, Alam A. Shafi, and Abdullah Badughaish. Cervical Thymic Cyst: A Unique Case Report with Related Embryogenesis. Science Repository, 2023. http://dx.doi.org/10.31487/j.jscr.2022.02.05.

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Cystic lesions of neck containing thymic tissue are rare and usually difficult to diagnose. Postulated hypothesis for this entity is the persistence and/or degeneration of thymopharyngeal duct derived from pharyngeal pouch endoderm. We report a unique case of persistent thymopharyngeal duct which was diagnosed antenatally at 30 weeks’ gestation, and it preserved its connection with the pharynx. Postnatal radiological studies were non-specific and misleading, and diagnosis was confirmed by histological examination of the excised specimen.
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4

Zhang, Ke, ZhongCai Tang, ZhaoXiong Yi, Yin Chen, ZhengMin Liu, and YanHong Bai. https://inplasy.com/inplasy-2022-11-0045. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.11.0045.

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Review question / Objective: The objective of this study was to evaluate the efficacy and safety of ultrasound-guided percutaneous lauromacrogol sclerotherapy for simple renal cysts. The analysis items included cyst volume reduction rate and complication rate. Condition being studied: Several strategies are available for the treatment of symptomatic simple renal cysts, however, there is no the most recommended treatment strategies. One of these strategies, ultrasound-guided percutaneous lauromacrogol sclerotherapy, is expected to become the most recommended treatment strategy.
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