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6 "Heterotopia"
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Case Studies
Colonic Adenocarcinoma Arising from Gastric Heterotopia: A Case Study
Hyoungsuk Ko, Shin Young Park, Eun Jung Cha, Jang Sihn Sohn
Korean J Pathol. 2013;47(3):289-292.   Published online June 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.289
  • 6,723 View
  • 41 Download
  • 16 Crossref
AbstractAbstract PDF

Heterotopic gastric mucosa occurs in all areas of the gastrointestinal tract including the nasopharynx, tongue, esophagus, small intestine, colon, and rectum. Gastric heterotopia of the large bowel is infrequent, and most cases have been reported in the rectum. Review of the literature has revealed only eight cases involving the colon proximal to the rectum. Little is known of the natural history of gastric heterotopias, except that. It usually presents with gastrointestinal bleeding, though other serious complications such as bowel perforation, intussusceptions, and fistula formation, are possible. Further, it is unclear whether heterotopic gastric mucosa progresses to malignancy. Herein, we describe a case of adenocarcinoma of the transverse colon arising from gastric heterotopia. To the best of our knowledge, this is the first report of adenocarcinoma arising from heterotopic gastric mucosa in the colon.

Citations

Citations to this article as recorded by  
  • Intussusception of Heterotopic Gastric Mucosa in the Transverse Colon: A Rare Cause of Perforation and Bleeding
    Sho Fujiwara, Ryuichi Nishimura, Nozomi Koyamada
    Cureus.2024;[Epub]     CrossRef
  • Gastric heterotopia of colon found cancer workup in liver abscess: A case report
    Jun Gi Park, Jeong Ill Suh, Yeo Un Kim
    World Journal of Clinical Cases.2022; 10(15): 5012.     CrossRef
  • Gastric heterotopia in the ileum mimicking Meckel's diverticulum
    Reza Shojaeian, Negar Nekooei, Paria Dehghanian
    Journal of Pediatric Surgery Case Reports.2022; 84: 102361.     CrossRef
  • Sometimes Things Are Not Where They Are Supposed to Be: A Case Report of Gastric Heterotopia in the Rectum
    Asher Lippe, Scott Lippe
    Physician's Journal of Medicine.2022;[Epub]     CrossRef
  • Gastric heterotopia of the rectum
    Eduardo Dantas, Diva Yamaguti, Kendi Yamazaki
    Gastroenterología y Hepatología.2021; 44(8): 579.     CrossRef
  • Bleeding Gastric Heterotopia of Cecal Diverticulum in an Adolescent: A Case Report
    Hyun-Il Seo, Jae-Young Kwak
    Advances in Pediatric Surgery.2021; 27(1): 32.     CrossRef
  • Gastric heterotopia of the rectum
    Eduardo Dantas, Diva Yamaguti, Kendi Yamazaki
    Gastroenterología y Hepatología (English Edition).2021; 44(8): 579.     CrossRef
  • Polypoid Gastric Heterotopia of Colon
    Marcela Adriana Duran Alvarez, Carla Noemi Tafur Sanchez
    GE - Portuguese Journal of Gastroenterology.2020; 27(1): 65.     CrossRef
  • Heterotopic Respiratory Mucosa in the Rectum: An Unusual Type and Site of Heterotopia in the Gastrointestinal Tract
    Caroline Bsirini, Pratyusha Tirumanisetty, Joseph N. Dytoc, Diana Agostini-Vulaj, Christopher Steevens, Asad Ullah, Aaron R. Huber
    International Journal of Surgical Pathology.2019; 27(2): 221.     CrossRef
  • Perforation of Heterotopic Gastric Mucosa in ileal duplication in an adult: A case report
    Vaanathi Paulvannan, Seshukumar Bylapudi, Mithun Kumar Ramesh Kumar, Mahesh Nachimuthu, Paulvannan Subramanian
    Journal of Surgical Case Reports.2019;[Epub]     CrossRef
  • Mixed adenoneuroendocrine carcinoma of the tongue arising within a congenital enteric cyst
    Louis J. Ligthelm, Belinda K. Bunn, Erich J. Raubenheimer, Willie F. P. van Heerden
    Head & Neck.2018;[Epub]     CrossRef
  • The outlet patch: gastric heterotopia of the colorectum and anus
    Abul A S R Mannan, Michael Vieth, Armen Khararjian, Binny Khandakar, Dora Lam‐Himlin, David Heydt, Feriyl Bhaijee, Henry J Venbrux, Kathleen Byrnes, Lysandra Voltaggio, Norman Barker, Songyang Yuan, Elizabeth A Montgomery
    Histopathology.2018; 73(2): 220.     CrossRef
  • Large heterotopic gastric mucosa and a concomitant diverticulum in the rectum: Clinical experience and endoscopic management
    Wen-Guo Chen, Hua-Tuo Zhu, Ming Yang, Guo-Qiang Xu, Li-Hua Chen, Hong-Tan Chen
    World Journal of Gastroenterology.2018; 24(30): 3462.     CrossRef
  • Gastric heterotopia in the rectum. A rare cause of ectopic gastric tissue
    George A. Salem, Javid Fazili, Tauseef Ali
    Arab Journal of Gastroenterology.2017; 18(1): 42.     CrossRef
  • Gastric heterotopia in rectum: A literature review and its diagnostic pitfall
    Peyman Dinarvand, Ashley A. Vareedayah, Nancy J Phillips, Christine Hachem, Jinping Lai
    SAGE Open Medical Case Reports.2017; 5: 2050313X1769396.     CrossRef
  • Heterotopic gastric mucosa in the anus and rectum: first case report of endoscopic submucosal dissection and systematic review
    Federico Iacopini, Takuji Gotoda, Walter Elisei, Patrizia Rigato, Fabrizio Montagnese, Yutaka Saito, Guido Costamagna, Giampaolo Iacopini
    Gastroenterology Report.2016; 4(3): 196.     CrossRef
Heterotopic Intestinal Cyst of the Submandibular Gland: A Case Study
Mi Jung Kwon, Dong Hoon Kim, Hye-Rim Park, Soo Kee Min, Jinwon Seo, Eun Soo Kim, Si Whan Kim, Bumjung Park
Korean J Pathol. 2013;47(3):279-283.   Published online June 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.279
  • 6,838 View
  • 39 Download
  • 5 Crossref
AbstractAbstract PDF

Heterotopic gastrointestinal cysts are rarely found in the oral cavity. Most of these cysts are lined with gastric mucosa and involve the tongue. There have been no reported heterotopic intestinal cysts of the submandibular gland that are completely lined with colonic mucosa. An 8-year-old girl presented with an enlarging swelling in the left submandibular area, and a 4-cm unilocular cyst was fully excised. The cyst was completely lined with colonic mucosa that was surrounded by smooth muscle layer, and the lining cells were positive for CDX-2, an intestinal marker, indicating a high degree of differentiation. The pathogenesis remains unclear, but it may be related to the misplacement of embryonic rests within the oral cavity during early fetal development. Although heterotopic intestinal cysts rarely occur in the submandibular gland, they should be considered in the differential diagnosis of facial swellings in the pediatric population.

Citations

Citations to this article as recorded by  
  • Heterotopic gastrointestinal cyst in the floor of mouth: a case report
    Naoaki SAITO, Satoshi MARUYAMA, Yusuke KATO, Ryoko TAKEUCHI, Jun-ichi TANUMA, Tadaharu KOBAYASHI
    Japanese Journal of Oral and Maxillofacial Surgery.2023; 69(1): 27.     CrossRef
  • A case report of oral heterotopic gastrointestinal cysts (HGIC) and review of the literature
    Gursimran Kaur Bains, Richard Pilkington, Joanna Stafford, Sunil Bhatia
    Oral Surgery.2022; 15(1): 71.     CrossRef
  • A Rare Case of Ectopic Colonic Mucosa Presenting With Airway Compromise in a Neonate
    Justin Hall, Fatima Z Aly, Julia Comer, Michael P Gebhard, Thomas Schrepfer
    Cureus.2022;[Epub]     CrossRef
  • Ultrasonic Features of Uncommon Congenital Heterotopic Colon and Pancreas in the Neck: An Extremely Rare Case Report
    Yingli Wei, Zhihao Pan, Xiaoling Kang, Cuiqing Huang, Dan Chen
    Frontiers in Pediatrics.2021;[Epub]     CrossRef
  • Quiste gastrointestinal heterotópico en la cavidad oral
    Beatriz Arango de Samper, Eliana Elisa Muñoz López, Estefanía Morales González
    Latin American Journal of Oral and Maxillofacial Surgery.2021; 1(1): 40.     CrossRef
Case Reports
Adenocarcinoma with Intraductal Papillary Mucinous Neoplasm Arising in Jejunal Heterotopic Pancreas
Ju Young Song, Jee Young Han, Sun Keun Choi, Lucia Kim, Suk Jin Choi, In Suh Park, Young Chae Chu, Kyu Ho Kim, Joon Mee Kim
Korean J Pathol. 2012;46(1):96-100.   Published online February 23, 2012
DOI: https://doi.org/10.4132/KoreanJPathol.2012.46.1.96
  • 8,109 View
  • 47 Download
  • 14 Crossref
AbstractAbstract PDF

A 74-year-old man suffered from jejunal perforation and adhesion to sigmoid colon due to adenocarcinoma associated with intraductal papillary mucinous neoplasm (IPMN) arising in a jejunal heterotopic pancreas. The jejunal lesion showed direct extension to the sigmoid colon, which was mistaken as sigmoid colon cancer by surgeons. Malignant transformation is a rare complication of a heterotopic pancreas. About half of malignancies in reported cases were ductal adenocarcinoma arising in the stomach, and the jejunal location is extremely rare. Furthermore, IPMN is also uncommon finding in a heterotopic pancreas.

Citations

Citations to this article as recorded by  
  • Intraductal Papillary Mucinous Neoplasm Arising from Heterotopic Pancreas in Stomach: A Case Report and Review of Literature
    Yu Pang, Yuyu Liu, Qinqin Liu, Gang Hou
    International Journal of Surgical Pathology.2023; 31(5): 708.     CrossRef
  • Clinicopathological features of intraductal papillary mucinous neoplasm derived from ectopic pancreas: A systematic review
    Jiro Kimura, Takehiro Okabayashi, Kenta Sui, Takahiro Murokawa, Motoyasu Tabuchi, Masaki Aida, Jun Iwata, Yasuhiro Hata
    Surgery Open Science.2022; 8: 62.     CrossRef
  • Clinicopathological Features of Intraductal Papillary Mucinous Neoplasm Derived from Ectopic Pancreas: A Systematic Review
    Jiro Kimura, Takehiro Okabayashi, Kenta Sui, Takahiro Murokawa, Motoyasu Tabuchi, Masaki Aida, Jun Iwata, Yasuhiro Hata
    SSRN Electronic Journal .2022;[Epub]     CrossRef
  • A case of ectopic pancreas of the stomach accompanied by intraductal papillary mucinous neoplasm with GNAS mutation
    Naoko Nambu, Takashi Yamasaki, Nami Nakagomi, Tsutomu Kumamoto, Tatsuro Nakamura, Akio Tamura, Toshihiko Tomita, Hiroto Miwa, Hisashi Shinohara, Seiichi Hirota
    World Journal of Surgical Oncology.2021;[Epub]     CrossRef
  • Intraductal Papillary Mucinous Neoplasm Arising in a Heterotopic Pancreas Treated by Percutaneous Endoscopic Intragastric Surgery
    Shoko Moue, Yoshimasa Akashi, Koichi Ogawa, Katsuji Hisakura, Tsuyoshi Enomoto, Yusuke Ohara, Yohei Owada, Shingo Sakashita, Tatsuya Oda
    The Japanese Journal of Gastroenterological Surgery.2020; 53(4): 371.     CrossRef
  • Adenocarcinoma with intraductal papillary mucinous neoplasm arising in a duodenal heterotopic pancreas: a case report
    Etsuko Hisanaga, Takaaki Sano, Norio Kubo, Norihiro Ishii, Ken Shirabe, Hitoshi Takagi, Junko Hirato, Hayato Ikota
    Clinical Journal of Gastroenterology.2020; 13(6): 1373.     CrossRef
  • Malignant Transformation of Ectopic Pancreas
    Irina M. Cazacu, Adriana Alexandra Luzuriaga Chavez, Graciela M. Nogueras Gonzalez, Adrian Saftoiu, Manoop S. Bhutani
    Digestive Diseases and Sciences.2019; 64(3): 655.     CrossRef
  • Anomalien im pankreatikobiliären System
    Dirk Walter, Michael Jung
    Der Gastroenterologe.2019; 14(4): 301.     CrossRef
  • Intraductal papillary mucinous neoplasm originating from a heterotopic pancreas within the jejunum: a case report
    Eiji Noda, Kenji Kuroda, Tomohisa Sera, Takuya Mori, Haruhito Kinoshita, Tsuyoshi Hasegawa, Hitoshi Teraoka, Takaaki Chikugo
    Journal of Surgical Case Reports.2018;[Epub]     CrossRef
  • Heterotopic Pancreas of the Gastrointestinal Tract and Associated Precursor and Cancerous Lesions
    Sun-Young Jun, Dahye Son, Mi-Ju Kim, Sung Joo Kim, Soyeon An, Young Soo Park, Sook Ryun Park, Kee Don Choi, Hwoon-Yong Jung, Song Cheol Kim, Jeong Hwan Yook, Byung-Sik Kim, Seung-Mo Hong
    American Journal of Surgical Pathology.2017; 41(6): 833.     CrossRef
  • Heterotopic Pancreas within the Proximal Hepatic Duct, Containing Intraductal Papillary Mucinous Neoplasm
    Alistair J. Lawrence, Aducio Thiessen, Amy Morse, A. M. James Shapiro
    Case Reports in Surgery.2015; 2015: 1.     CrossRef
  • Bowel Rest
    Payal Saxena, Deborah Belchis, Anne Marie Lennon
    Clinical Gastroenterology and Hepatology.2015; 13(13): e173.     CrossRef
  • Adenocarcinoma arising from jejunal ectopic pancreas mimicking peritoneal metastasis from colon cancer: a case report and literature review
    Yusuke Yamaoka, Tomohiro Yamaguchi, Yusuke Kinugasa, Akio Shiomi, Hiroyasu Kagawa, Yushi Yamakawa, Masakatsu Numata, Shinya Sugimoto, Kenichiro Imai, Kinichi Hotta, Keiko Sasaki
    Surgical Case Reports.2015;[Epub]     CrossRef
  • Intraductal papillary mucinous neoplasm of the ileal heterotopic pancreas in a patient with hereditary non-polyposis colorectal cancer: A case report
    Sang Hwa Lee
    World Journal of Gastroenterology.2015; 21(25): 7916.     CrossRef
Nasal Cerebral Heterotopia-so called Nasal Glioma: A case report.
Tae Sook Kim, Je G Chi
Korean J Pathol. 1995;29(4):517-520.
  • 1,404 View
  • 17 Download
AbstractAbstract PDF
Encephalocele and nasal glioma are rare, benign congenital neuroectodennal tumors which result from a failure of embryologic sepearation of neuroectodermal and ectodemlal tissues. Nasal glioma should be differentiated from a true glioma, and from a primary encephalocele, which is a herniation of the cranial contents through a bony defect in the skull. For this reason, nasal cerebral heterotopia is a preferred term. We report an unusual case of a nasal mass that was histologically indistinguishable from nasal cerebral heterotopia but proved to be connected to the skull base by fibrotic cord. The patient was a 2 year old girl who had had a slow growing palpable mass in the left epicanthal area for three months.
Heterotopic Brain Tissue in the Soft Palate.
Hyun Joo Choi, Youn Soo Lee, Young Shin Kim, Kyo Young Kim, Chang Suk Kang, Sang In Shim
Korean J Pathol. 1998;32(11):1039-1041.
  • 1,623 View
  • 10 Download
AbstractAbstract
Heterotopic brain tissue is a developmental anomaly of neurogenic origin with no malignant potential, and is usually present around the nose of children and infants. So it has been called nasal glioma. But, even more rarely, heterotopic glial tissue may be found in various sites other than nasal cavity, such as the ethmoidal sinus, palate, tonsillar area, pharynx, ear, subcutaneous tissue, lung, and female genital tract. We experienced a more unusual case of a polypoid heterotopic brain tissue in the soft palate in a 3-year-old boy. The mass was microscopically reminiscent of "gliosis" of the central nervous system and interestingly contained choroid plexus focally. The glial nature of the lesion was confirmed by glial fibrillary acidic protein immunostain.
Hemimegalencephaly: A case report.
Youn Soo Lee, Eun Sun Jung, Sun Moo Kim, Byung Kee Kim
Korean J Pathol. 2000;34(3):243-247.
  • 1,641 View
  • 19 Download
AbstractAbstract PDF
Hemimegalencephaly is an uncommon sporadic congenital malformation of the central nervous system characterized by enlargement of one cerebral hemisphere with cranial asymmetry, hemiparesis, epilepsy, and mental retardation. This report deals with a 12-month-old girl with intractable seizure and developmental delay, who revealed hemispheric asymmetry and enlarged right cerebral hemisphere. MRI scan revealed asymmetric enlargement of right cerebral hemisphere with lissencephaly and multifocal calcification. She underwent right frontal lobectomy and parietal cortical resection, but died of complication of surgery. Histological features included loss of cortical lamination, large atypical neurons, neuronal heterotopia, and astrocytosis with dystrophic calcification. The heterotopic neurons in the white matter were suggestive of aberrant neuronal migration.

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