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Journal articles on the topic 'Rare cyst'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Jain, Leena, Ashish K. Maurya, Shalini Jadia, and Sadat Qureshi. "Sublingual Epidermoid Cyst: A Rare Presentation." International Journal of Advanced and Integrated Medical Sciences 1, no. 4 (2016): 194–95. http://dx.doi.org/10.5005/jp-journals-10050-10061.

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ABSTRACT Infection of pilo-sebacious gland or traumatic migration of epidermis to the deeper layers of the skin can lead to epidermoid cyst. Any site of the body which is lined by squamous epithelium can be the site of epidermoid cyst. We present a case of sublingual epidermoid cyst in a 14-year-old female, who presented with a slow-growing, soft, midline swelling in submental region. Cyst was excised under local anesthesia with sedation. Histopathological examination revealed a cystic wall lined by keratinizing squamous epithelium with lamellated keratin and fibrocollagenous tissue with conge

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12

Rijhsinghani, Archana N. "Teratoid Cyst with Nephrogenic Elements: A Rare Case." Annals of Pathology and Laboratory Medicine 7, no. 11 (2020): C160–163. http://dx.doi.org/10.21276/apalm.2902.

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Teratoid cyst is a type of dermoid cyst, the lining of which varies from stratified squamous to a ciliated respiratory epithelium containing derivatives of ectoderm, mesoderm and endoderm. The most common location of this cyst is oral cavity and presence of nephrogenic elements has been very rarely reported. We report a very uncommon rare case of teratoid cyst with nephrogenic elements in cyst wall and intestinal duplication cyst in a 6-month-old-female child.

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13

Ruchi Agarwal, Swaran Kaur, Parul, Parveen Rana, Kulwant Singh, and Monika Gathwal. "Splenic epithelial cyst: A rare entity on autopsy." Indian Journal of Forensic Medicine & Toxicology 18, no. 3 (2024): 13–16. http://dx.doi.org/10.37506/rw6nnj22.

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INTRODUCTION Splenic cyst is a rare entity with very few cases reported in literature. The diagnosis is usually incidental on autopsy, associated with symptoms due to enlargement, rupture, infection, or hemorrhage. It can be of two types - parasitic or non parasitic cyst. CASE REPORT Post mortem viscera of 33 year old male were received in the department of Pathology for histopathological examination. Grossly, an enlarged spleen weighing 180 gm and measuring 9x8x6 cm was identified. On cut section, an eccentric unilocular cyst measuring 7x6 cm was identified. The cyst was filled with brownish

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14

Nilesh, Kumar. "Nasolabial cyst: a rare non-odontogenic orofacial cyst." BMJ Case Reports 13, no. 6 (2020): e235621. http://dx.doi.org/10.1136/bcr-2020-235621.

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15

Hawary, Amr, and Peter Duffy. "Urachal Cyst, a Rare Cyst with Multiple Complications." Scientific World JOURNAL 8 (2008): 237–38. http://dx.doi.org/10.1100/tsw.2008.45.

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Urachal cysts are rare, can be one of the forgotten causes of abdominal pain, and can present as adenocarcinoma of the bladder, along with many other presentations. There is a real need for physicians, general surgeons, and urologists to be acquainted with the different presentations and management of this rare condition.

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16

Chaabouni, Mohamed Amine, Imen Achour, Wadii Thabet, et al. "Parathyroid cyst: A rare entity." SAGE Open Medical Case Reports 9 (January 2021): 2050313X2110666. http://dx.doi.org/10.1177/2050313x211066648.

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Parathyroid cysts are an uncommon entity. They are classified as functioning and nonfunctioning cysts. Cyst aspiration with detection of parathyroid hormone is a useful tool to confirm the diagnosis. Here, we report four cases of parathyroid cysts. One patient had a functioning cyst. Ultrasonography of the neck revealed a cystic lesion behind the left lobe of the thyroid gland in two cases and a right cystic thyroid nodule in two cases. The cysts exerted a mass effect on the adjacent structures in two cases without clinical compressive symptoms. Fine-needle aspiration with detection of parathy

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17

Sable, Shailesh, Jyoti Mehta, Sudeep Yadav, Priyadarshan Jategaokar, and Premashish J. Haldar. "“Primary Omental Hydatid Cyst”: A Rare Entity." Case Reports in Surgery 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/654282.

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Hydatid cyst is caused by the parasiteEchinococcus granulosuscommonly seen in temperate regions. Primary omental hydatid cyst is rare entity. Diagnosis can be achieved with contrast-enhanced computed tomography of abdomen and pelvis along with serology. Eosinophilia is a strong pointer to hydatid cyst as a differential diagnosis. Open or laparoscopic excision of the cyst along with medical therapy remains the treatment of choice.

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18

Subedi, Kirtipal, Karishma Vaidhya, Bigya Shrestha, and Kamana KC. "Primary Pelvic Hydatid Cyst: a Rare Case." Nepal Journal of Obstetrics and Gynaecology 13, no. 3 (2018): 66. http://dx.doi.org/10.3126/njog.v13i3.23510.

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Hydatid cyst is ecchinococcal disease caused by tapeworm echinococcus, most commonly by metacestode stage of echinococcus granulosus. Liver is the most common organ to be aff ected followed by lungs and spleen. Primary hydatid cyst in the pelvis is rare. We report a case of primary isolated pelvic hydatid cyst diagnosed incidentally during laparotomy performed for adnexal mass. Key words: adnexae, albendazole, echinococcus, hydatid cyst, laparotomy

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19

El Khassoui, Amine, El Mouhtadi Aghoutane, Tarik Salama, and Redouane El Fezzazi. "Psoas Hydatid Cyst in Children: A Rare Localization about a Case." Case Reports in Pediatrics 2021 (November 6, 2021): 1–3. http://dx.doi.org/10.1155/2021/1961509.

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Introduction. The development of hydatid cysts in the muscle is rare, and it is even rarer in children. We report the case of a 9-year-old child treated in pediatric orthopedics department at the University Hospital of Marrakech for a hydatid cyst psoas muscle revealed by lameness. Result. The child was consulted for painless and afebrile lameness of the left hip evolving since 3 months. The clinical examination finds a mass of the left flank. Investigations based on the abdominal ultrasound in first intention showed a hydatid cyst depending on the left psoas muscle. Pelvic CT and abdominal MR

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20

Pushpalatha, Dr D. "Cyst In Mediastinum – A Rare Case Report." Journal of Medical Science And clinical Research 04, no. 12 (2016): 14454–57. http://dx.doi.org/10.18535/jmscr/v4i12.26.

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21

Jain, Kanika. "A Rare Congenital Anomaly: Jejunal Duplication Cyst." Recent Advances in Pathology & Laboratory Medicine 05, no. 02 (2019): 27–30. http://dx.doi.org/10.24321/2454.8642.201911.

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22

Rathour, Devesha, and Aborishi Garg. "Rare Case of Hydatid Cyst of Breast." International Journal of Science and Research (IJSR) 11, no. 7 (2022): 16–18. http://dx.doi.org/10.21275/sr22628230920.

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23

P G, Aiswarya, and Laila Raji N. "Pleuropericardial Cyst - A Rare Tumour of Mediastinum." International Journal of Science and Research (IJSR) 13, no. 12 (2024): 600–602. https://doi.org/10.21275/sr241207205119.

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24

S, Prabhu, Mhaske Shubhangi, Maheshwari Ashish, and Jha Prabhu Shweta. "Nasolabial Cyst: A Diagnostic Clarity or Conundrum?" PJSR 9, no. 1 (2016): 61–64. https://doi.org/10.5281/zenodo.8247546.

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Nasolabial cyst is a unique, rare, non odontogenic cyst occurring in nasal alar region. It has a predeliction for females with the left side being more affected than the right. Patients generally present with a painless slow growing swelling in the alar region without significant radiographic abnormality. This paper discusses a case of nasolabial cyst in a 45 year old female patient

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25

Gupta, Siddharth. "Ameloblastomatous Calcifying Odontogenic Cyst: A Rare Clinicopathologic Entity." International Journal of Head and Neck Surgery 2, no. 2 (2011): 115–18. http://dx.doi.org/10.5005/jp-journals-10001-1063.

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ABSTRACT The calcifying odontogenic cyst represents a heterogeneous group of lesions that exhibits a variety of clinicopathologic and behavioral features. Therefore, a proper categorization of the cases is needed for better understanding of each variant. Ameloblastoma is one of the well-known odontogenic tumors that could be associated with calcifying odontogenic cyst. Very few cases of ameloblastomatous calcifying odontogenic cyst have been reported in the literature. In this report, we present a case of ameloblastomatous calcifying odontogenic cyst differentiating it from other variants of c

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26

Sangani, Viral G., Aasit L. Pathak, Bhupesh Patel, and Aayushi Pugaliya. "Choledochal cyst type VI: a rare case report." International Surgery Journal 11, no. 9 (2024): 1534–37. http://dx.doi.org/10.18203/2349-2902.isj20242456.

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Choledochal cyst or biliary cyst is a congenital anomaly affecting the biliary tree. It involves the dilatation of the biliary tree that could affect the extra hepatic and/or the intrahepatic segments. We present a 40 year old female with constant right upper abdominal pain, diagnosed with choledochal cyst. She underwent laparoscopic cholecystectomy with choledochal cyst (CDC) excision. She was uneventful postoperatively and then discharged.

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27

Bhatt, Vinay S., Greeshma P G, Famida P A, and Reshma Radhakrishnan. "A rare case of paediatric sublingual keratinous cyst." IP Indian Journal of Anatomy and Surgery of Head, Neck and Brain 8, no. 4 (2023): 133–38. http://dx.doi.org/10.18231/j.ijashnb.2022.032.

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The occurrence of keratinous cyst in the oral cavity is extremely rare. Keratinous cyst in the floor of the mouth is painless, doughy or fluctuant lesion and causes no symptoms until it is large enough to interfere with speech or eating. Cyst generally presents as slow and progressive growth and often not diagnosed until the second or third decade of life.We report an uncommon presentation of keratinous cyst of the sublingual space in a 6year old female child. The swelling was mimicking ranula on inspection. On complete examination, the swelling appeared as epidermoid cyst. After a routine eva

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28

Maddi, Lavanya, Dilip Kumar Mishra, and Swathi Kaliki. "Fungal dacryops: a rare presentation." BMJ Case Reports 18, no. 2 (2025): e261168. https://doi.org/10.1136/bcr-2024-261168.

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A woman in her late 40s presented with a cystic lesion in the left lacrimal gland for 1 year and associated pain in the past 3 months. On examination, the patient had cystic lesion in the left lacrimal gland region without any signs of inflammation. An initial provisional diagnosis of simple dacryops of the left eye was made, and the lesion was observed. On review at 1 month, the patient complained of persistent swelling and dull pain in the left eye. Excisional biopsy of the lesion was planned. Intraoperatively, the cyst ruptured during surgery, and yellowish, granule-like concretions were no

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29

Narwal, Anjali, Anju Devi, AchlaBharti Yadav, Virender Singh, and Ambika Gupta. "Report of a rare cyst at a rare site: Heterotopic gastrointestinal cyst partially lined with dermoid cyst epithelium." National Journal of Maxillofacial Surgery 8, no. 1 (2017): 81. http://dx.doi.org/10.4103/njms.njms_67_15.

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30

Singh, Sanjay, and Mahesh Reddy. "A rare case of primary peritoneal hydatid cyst." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 1 (2016): 360. http://dx.doi.org/10.18203/2320-1770.ijrcog20164698.

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Primary peritoneal hydatid cyst is a rare entity. A 42 yr old parous female presented with painless lower abdominal lump since 6 months. On clinical examination an immobile abdominopelvic lump of the size of 18-20 weeks pregnant uterus with bosselated surface was noted. Ultrasound Sonography Test (USG) and Contrast Enhanced Computerized Tomography Scan (CECT scan) of abdomen and pelvis revealed large multilocular abdominopelvic cystic mass in continuity with RT ovary. Radiologically a differential diagnosis of hydatid cyst and mucinous cystadenoma was made. All relevant ovarian tumor markers w

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31

Chincholkar, Rajesh G., and Ram V. Tongale. "Primary hydatidosis of psoas muscle: rare entity." International Surgery Journal 9, no. 5 (2022): 1110. http://dx.doi.org/10.18203/2349-2902.isj20221168.

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Hydatid cyst of the psoas is uncommon to see. We hereby report a case of hydatid cyst of the psoas in a 22 years old female patient presented with pain and swelling in right lumber region. CECT abdomen revealed hydatid cyst indenting inferior pole of right kidney also indenting adjacent ascending colon and abutting right psoas muscle.

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32

Chincholkar, Rajesh G., and Ram V. Tongale. "Primary hydatidosis of psoas muscle: rare entity." International Surgery Journal 9, no. 5 (2022): 1110. http://dx.doi.org/10.18203/2349-2902.isj20221168.

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Hydatid cyst of the psoas is uncommon to see. We hereby report a case of hydatid cyst of the psoas in a 22 years old female patient presented with pain and swelling in right lumber region. CECT abdomen revealed hydatid cyst indenting inferior pole of right kidney also indenting adjacent ascending colon and abutting right psoas muscle.

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33

Neyaz, Zafar, Surya Nandan Prasad, Vivek Singh, and Rajendra Vishnu Phadke. "Repeated aspiration and sclerotherapy to manage recurrent spinal epidermoid cyst." BMJ Case Reports 14, no. 7 (2021): e239730. http://dx.doi.org/10.1136/bcr-2020-239730.

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Spinal epidermoid cysts are rare lesions and epidermoid cyst in intramedullary location is even rarer. Surgical excision is the mainstay of treatment; however, in cases of recurrence, repeat surgery becomes quite difficult. Treatment of recurrent intramedullary epidermoid cyst by surgery alone is a challenge. We managed one such rare case with repeated aspiration and sclerotherapy. Here, we have highlighted hypertonic saline sclerotherapy as a promising tool to treat recurrent spinal epidermoid cysts.

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34

Singh, Dr Shashikant. "Perianal Parasitic Cyst in a Child – Case Report." Journal of Medical Science and clinical Research 13, no. 05 (2025): 25–29. https://doi.org/10.18535/jmscr/v13i05.04.

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Perianal cyst in pediatric age group is very rare, even rarer is a parasitic cyst in perianal region. Epidermoid cyst or a parasitic cyst may present in perianal region. Epidermoid cysts are common skin lesions. They can get complicated by inflammation, infection, rupture, or malignancy. Parasitic cyst may be caused by Enterobius vermicularis, Strongyloides and Echinococcus granulosus. They present as a cyst, nodule, granuloma or as an abscess. These cysts are not common in children and scarcely reported. We herein report a case of Perianal parasitic Cyst in a 5 year old boy who was successful

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35

Loganathan, Mahalakshmi, Prasad Harikrishnan, Rajmohan Muthusamy, and Senthilkumar Nagarajan. "Dentigerous Cyst Associated with Compound Odontome in the Anterior Region of Maxilla – A Case Report." Journal of Pierre Fauchard Academy (India Section) 35, no. 4 (2022): 144. http://dx.doi.org/10.18311/jpfa/2021/28690.

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Dental professionals encountered tumor and cystic lesions in their daily practice. However, a concurrent lesion are quite rare and poses diagnostic challenge. Odontoma are the most common odontogenic tumor of the jaw. Although transformation from cyst to tumor is quite common (orgin of ameloblastoma from a dentigerous cyst) but tumor to cyst is very rare1. Here, we report a case of a dentigerous cyst associated with odontome and an unerupted tooth in the anterior region of the maxilla.

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36

Shin, John Junghun, Ki-Yeon Kwon, and Jin-Rok Oh. "INTRAOSSEOUS EPIDERMOID CYST DISCOVERED IN THE DISTAL PHALANX OF A THUMB: A CASE REPORT." Hand Surgery 19, no. 02 (2014): 265–67. http://dx.doi.org/10.1142/s0218810414720241.

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Intraosseous epidermoid cyst is considered a rare benign inclusion cyst found mainly in the skull and phalanges. Once the cyst is differentiated from other similar lesions, the cyst can be treated with simple curettage, seldom requiring additional managements. We experienced this rare case that had been treated successfully without complication.

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37

Ozbek, O., K. Odev, Y. Solak, B. Fevzioglu, and I. Guler. "An exceedingly rare type of renal cyst: amoebic cyst." QJM 106, no. 3 (2012): 281–82. http://dx.doi.org/10.1093/qjmed/hcs005.

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38

Jaakik, Btissam, and Houda Benjelloun. "A Rare Pericardial Cyst Resembling Hydatid Cyst on Echocardiography." Internal Medicine 49, no. 15 (2010): 1673–74. http://dx.doi.org/10.2169/internalmedicine.49.3764.

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39

Patil, Prachi Prabhakar, Meena Satia, and V. Badhwar. "A rare case of hydrocele in a female." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 3 (2019): 1215. http://dx.doi.org/10.18203/2320-1770.ijrcog20190910.

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Vulval swellings have always been a case of a difficult and a puzzling situation and more so when they are huge in size. Vulvar swellings are of various types such as Bartholin cyst, sebaceous cyst, cyst of canal of nuck, inguino-labial hernia and vulval varicosities. Most common vulvar cysts are epidermal inclusion cysts. Usual location is beneath the epidermis. An alternative histogenesis is embryonic remnants or occlusion of pilosebaceous ducts of sweat glands. Cutaneous cysts which are lined by ciliated epithelium are very rare, and authors present a rare case of a cyst arising from a left

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40

Singh, Anil Kumar, Priyanka Gogoi, Preeti Diwaker, Bhuvan Adhlakha, and Aishwary Gayatree. "Osseous metaplasia of ovarian cyst: a rare case report." International Surgery Journal 5, no. 9 (2018): 3164. http://dx.doi.org/10.18203/2349-2902.isj20183741.

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Osseous metaplasia has been described at many sites, however previous reports of osseous metaplasia in ovarian lesions are rare. This is most commonly associated with dermoid cyst, osseous metaplasia in stroma rich in serous or mucinous neoplasm and ossification of endometriotic cyst (chocolate cyst). Here The authors report a case of incidental finding of osseous metaplasia in the endometriotic cyst (chocolate cyst) of resected ovary in 42-year-old female who had gone for total abdominal hysterectomy with bilateral salpingo-oophorectomy for provisional diagnosis of AUB.

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41

Cicciù, Marco, Giovanni Battista Grossi, Andrea Borgonovo, Giacomo Santoro, Francesco Pallotti, and Carlo Maiorana. "Rare Bilateral Nasopalatine Duct Cysts: A Case Report." Open Dentistry Journal 4, no. 1 (2010): 8–12. http://dx.doi.org/10.2174/1874210601004010008.

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The nasopalatine duct cyst (NPDC) is the most common of the non-odontogenic cyst of the jaws. This cysts are usually central or unilateral with no prevalence of side occurrence. The NPDC is the most frequent developmental, nonodontogenic cyst of the jaws. This cyst originates from epithelial remnants from the nasopalatine duct. The cells could be activated spontaneously during life, or are eventually stimulated by the irritating action of various agents (infection, etc.). Generally, patients present without clinical signs and symptoms. Therefore, the tentative diagnosis "nasopalatine duct cyst

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42

NB, Nagaveni, and Parashar K. "Incisive Canal Cyst (Nasopalatine Duct Cyst) in a Pediatric Patient – A Rare Case Report." Clinical Pathology & Research Journal 8, no. 1 (2024): 1–4. https://doi.org/10.23880/cprj-16000210.

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Incisive canal cyst also called as Nasopalatine duct cyst is a rare non-odontogenic and non-neoplastic cyst occurring in the oral cavity. The most common occurrence in the general population usually varies from third to sixth decade. Development of this cyst is uncommon in children. Therefore, the aim of this case publication is to report an occurrence of incisive canal cyst in a 14-year-old Indian male patient. As this cyst is asymptomatic and painless most of the time it is accidentally diagnosed following a radiographic examination. Therefore, knowledge about its occurrence, diagnosis and m

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43

Bansal, Anshul, and Parul Bansal. "NASOALVEOLAR CYST: A RARE ENTITY." Journal of Evolution of Medical and Dental Sciences 2, no. 40 (2013): 7777–80. http://dx.doi.org/10.14260/jemds/1373.

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44

Hyo, Yukihiko, Shigeru Inafuku, Hiromichi Ishigami, Isao Takimoto, and Hiroshi Iwasaki. "A Rare Thyroglossal Duct Cyst." Practica oto-rhino-laryngologica. Suppl. 1994, Supplement73 (1994): 138–41. http://dx.doi.org/10.5631/jibirinsuppl1986.1994.supplement73_138.

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45

Shekhar, Chandra, Kranti Bhavana, and Sarita Kumari Mishra. "Dentigerous cyst: A rare presentation." Indian Journal of Otolaryngology and Head and Neck Surgery 58, no. 4 (2006): 382–84. http://dx.doi.org/10.1007/bf03049603.

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46

HERRERA-ZAMORA, JULIO, PATRICIO SANTILLAN-DOHERTY, GUILLERMO PONCE-DE-LEON-BALLESTEROS, and FRANCINA BOLANOS. "RARE ESOPHAGEAL BRONCHOGENIC CYST MANAGMENT." Chest 154, no. 4 (2018): 40A. http://dx.doi.org/10.1016/j.chest.2018.08.037.

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Baskan, Müslüm Gökhan. "A RARE CAUSE OF TENSION PNEUMOTHORAX ECHINOCOCCUS GRANULOSUS." Archives of Current Medical Research 6, no. 1 (2025): 59–65. https://doi.org/10.47482/acmr.1516440.

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Hydatid cyst (HH) is a zoonotic parasitic disease caused by Echinococcus. The most common site of localization is the liver and the second most common site is the lungs. The most common complication of pulmonary hydatid cyst is rupture of the cyst into the bronchus. Tension pneumothorax is a very rare complication. The diagnosis of hydatid cyst of the lung is based on clinical and radiologic imaging methods and serologic tests. Treatment is primarily surgical. In this case, we aimed to present a case of an adult patient who presented with tension pneumothorax, in which the diagnosis of hydatid

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Choi, Ji Eun, Ho Jun Seol, and Yang-Sun Cho. "Giant petroclival endodermal cyst with xanthogranulomatous changes." Journal of Neurosurgery: Pediatrics 12, no. 3 (2013): 284–87. http://dx.doi.org/10.3171/2013.6.peds1362.

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Endodermal cyst is a rare developmental cyst of the CNS, such as a Rathke cleft and colloid cyst lined by columnar epithelium of presumed endodermal origin. Intracranial endodermal cysts are rare, and most are found in the posterior fossa. The authors report a case of petroclival endodermal cyst with extensive bone destruction. A 12-year-old boy presented with transient facial weakness and headache. Imaging revealed a 3 × 3 × 4–cm, partial rim, enhanced cystic lesion in the petroclival area that was isointense on T1-weighted imaging and hyperintense in T2-weighted imaging. The cyst wall was pa

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Singh, Dr Shubhanshi, Dr Neha Agarwal, Dr Sarah Afaque, Dr Somi Fatima, and Dr Madhulika Chandel. "Diagnostic Dilemma -Pericoronitis or Unicystic Ameloblatoma: A Rare Case Report." Saudi Journal of Oral and Dental Research 10, no. 06 (2025): 255–59. https://doi.org/10.36348/sjodr.2025.v10i06.001.

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Dentigerous cyst (DCs) is the type of odontogenic cyst and is the one of the most common type of cyst occurring in the jaw. Dentigerous cyst is clinically asymptomatic and is found radiographically. It encloses the crown of impacted tooth. Histological evaluation is important in such cases as sometimes radiographically interpretated Dentigerous cyst is diagnosed as Unicystic ameloblastoma, dental follicle or an odontogenic keratocyst. In this case report, 18years old boy is reported with clinical diagnosis of pericoronitis and radiographic finding of Dentigerous cyst which on histopathological

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Bhadani, Punam Prasad, S. P. Sah, and A. Afaque. "EPIDERMOID CYST OF THE SPLEEN: REPORT OF A CASE." Journal of Nepal Medical Association 42, no. 149 (2003): 297–99. http://dx.doi.org/10.31729/jnma.649.

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Splenic epidermoid cyst is a rare entity and represents about 10% of the non-parasitic benign cysts of thespleen. We report a rare case of epidermoid cyst in a 45-year-old female who presented with pain and leftupper abdominal mass. So far, such case has not been reported from Nepal.Key Words: Epidermoid cyst, spleen, late onset, mesothelial cyst.

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