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1. エキノコックス症の臨床症状および診断clinical manifestations and diagnosis of echinococcosis [show details]
…"water-lily" sign for floating membranes, and CE3b, which is predominantly solid with daughter cysts. Establishing whether daughter cysts are present is important for guiding treatment. In addition, nuclear magnetic …
2. エキノコックス症の治療および予防treatment of echinococcosis [show details]
…and CE3b cysts (which may contain daughter cysts). Establishing whether daughter cysts are present is important for guiding treatment, since the presence of daughter cysts reduces the likelihood of successful …
3. 胆嚢嚢胞biliary cysts [show details]
4. エキノコックス症の疫学および制御epidemiology and control of echinococcosis [show details]
…hydatid fluid and small secondary cysts (brood capsules), which bud internally from this layer. Fragmentation of the germinative layer and brood capsules gives rise to daughter cysts. These may develop within …
5. 胆道寄生虫症の内視鏡診断およびマネージメントendoscopic diagnosis and management of biliary parasitosis [show details]
…frank intrabiliary ruptures are usually symptomatic. The contents of the cyst (the scolices and daughter cysts) drain into the biliary ducts and cause intermittent or complete obstruction of bile duct, resulting …

van Asselt SJ1, Brouwers AH2, van Dullemen HM3, van der Jagt EJ4, Bongaerts AH5, Koopmans KP6, Kema IP7, Zonnenberg BA8, Timmers HJ9, de Herder WW10, Sluiter WJ11, de Vries EG12, Links TP13.
European journal of endocrinology / European Federation of Endocrine Societies.Eur J Endocrinol.2016 May;174(5):611-20. doi: 10.1530/EJE-15-1012. Epub 2016 Feb 16.
BACKGROUND: Patients with von Hippel-Lindau (VHL) disease are prone to develop pancreatic neuroendocrine tumors (pNETs). However, the best imaging technique for early detection of pNETs in VHL is currently unknown. In a head-to-head comparison, we evaluated endoscopic ultrasound (EUS) and (11)C-5-hy
PMID 26884551

The C175R mutation alters nuclear localization and transcriptional activity of the nephronophthisis NPHP7 gene product.

Ramachandran H1, Yakulov TA1, Engel C1, Müller B1, Walz G1,2.
European journal of human genetics : EJHG.Eur J Hum Genet.2016 May;24(5):774-8. doi: 10.1038/ejhg.2015.199. Epub 2015 Sep 16.
Nephronophthisis (NPH) is a rare autosomal ciliopathy, but the leading cause for hereditary end-stage renal disease in children. Most NPH family members form large protein networks, which appear to participate in structural elements of the cilium and/or function to restrict access of molecules to th
PMID 26374130

Daughter and Mother with Orofaciodigital Syndrome Type 1 and Glomerulocystic Kidney Disease.

Iijima T1, Hoshino J2, Mise K1, Sumida K1, Suwabe T1, Hayami N1, Ueno T1, Takaichi K3, Fujii T4, Ohashi K5, Morisada N6, Iijima K6, Ubara Y3.
Human pathology.Hum Pathol.2016 Apr 27. pii: S0046-8177(16)30045-4. doi: 10.1016/j.humpath.2016.04.005. [Epub ahead of print]
A 35-year-old woman was admitted to our hospital for evaluation of end-stage renal failure. Diagnostic imaging, including ultrasonography and MRI, showed polycystic kidneys and peribiliary hepatic cysts, but the renal cysts were isointense and her kidneys were smaller than the end-stage kidneys of p
PMID 27131853

A large functioning parathyroid cyst in a patient with multiple endocrine neoplasia type 1

Tamiya Hiroyuki,Miyakawa Megumi,Suzuki Hisanori,Takeshita Akira,Ohashi Kenichi,Usui Takeshi,Miura Daishu,Takeuchi Yasuhiro
Endocrine Journal 60(6), 709-714, 2013
… Further, a prolactinoma was detected, and the patient's son and daughter also had primary hyperparathyroidism, indicating that the patient had multiple endocrine neoplasia type 1 (MEN1). … After parathyroidectomy with autotransplantation, the largest cystic mass, in the left lower thyroid lobe, was pathologically diagnosed as a functioning parathyroid cyst, and all laboratory data returned to normal. …
NAID 130004443886

A Pathomorphological Study of Fractal Analysis in Parenchymal-stromal Border on Keratocystic Odontogenic Tumor—with Special Reference to Proliferative Activity and Vascular Distribution—

Suemitsu Masaaki
International Journal of Oral-Medical Sciences 10(4), 372-383, 2012
… Keratocystic odontogenic tumor shows a relatively high rate of recurrence with daughter cysts and epithelial islands. … Determining evidence of the daughter cysts or epithelial islands is therefore important for deciding treatment and assessing the prognosis. …
NAID 130002051673

田中章夫,González-Alva Patricia,田中真,坂下英明,草間薫
小児口腔外科 18(1), 9-14, 2008
… The thin lining epithelium frequently separates from the underlying connective tissue, and is one of the causes of recurrence as well as daughter cyst and epithelial rests. … A cystic lesion in which the whole lining epithelium shows orthokeratinization is referred to as orthokeratinized odontogenic cyst and should be separated from KCOT because recurrence is rare. …
NAID 130004356848