Bowel “Dissection” in Microvillus Inclusion Disease
A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the ba...
Ausführliche Beschreibung
Autor*in: |
Ming-Chou Chiang [verfasserIn] Jen-Fu Hsu [verfasserIn] Chuen Hsueh [verfasserIn] Hsun-Chin Chao [verfasserIn] Tzu-Hao Wang [verfasserIn] Chih-Ping Chen [verfasserIn] Ming-Wei Lai [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2015 |
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Übergeordnetes Werk: |
In: Pediatrics and Neonatology - Elsevier, 2017, 56(2015), 2, Seite 129-131 |
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Übergeordnetes Werk: |
volume:56 ; year:2015 ; number:2 ; pages:129-131 |
Links: |
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DOI / URN: |
10.1016/j.pedneo.2013.03.004 |
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Katalog-ID: |
DOAJ035796553 |
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520 | |a A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. | ||
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10.1016/j.pedneo.2013.03.004 doi (DE-627)DOAJ035796553 (DE-599)DOAJcc78978685504501baa2c6f87141d22c DE-627 ger DE-627 rakwb eng RJ1-570 Ming-Chou Chiang verfasserin aut Bowel “Dissection” in Microvillus Inclusion Disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. antenatal intestinal obstruction diarrhea dissection microvillus inclusion disease (MVID) Pediatrics Jen-Fu Hsu verfasserin aut Chuen Hsueh verfasserin aut Hsun-Chin Chao verfasserin aut Tzu-Hao Wang verfasserin aut Chih-Ping Chen verfasserin aut Ming-Wei Lai verfasserin aut In Pediatrics and Neonatology Elsevier, 2017 56(2015), 2, Seite 129-131 (DE-627)573750971 (DE-600)2441821-3 18759572 nnns volume:56 year:2015 number:2 pages:129-131 https://doi.org/10.1016/j.pedneo.2013.03.004 kostenfrei https://doaj.org/article/cc78978685504501baa2c6f87141d22c kostenfrei http://www.sciencedirect.com/science/article/pii/S1875957213000399 kostenfrei https://doaj.org/toc/1875-9572 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2004 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 56 2015 2 129-131 |
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10.1016/j.pedneo.2013.03.004 doi (DE-627)DOAJ035796553 (DE-599)DOAJcc78978685504501baa2c6f87141d22c DE-627 ger DE-627 rakwb eng RJ1-570 Ming-Chou Chiang verfasserin aut Bowel “Dissection” in Microvillus Inclusion Disease 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. antenatal intestinal obstruction diarrhea dissection microvillus inclusion disease (MVID) Pediatrics Jen-Fu Hsu verfasserin aut Chuen Hsueh verfasserin aut Hsun-Chin Chao verfasserin aut Tzu-Hao Wang verfasserin aut Chih-Ping Chen verfasserin aut Ming-Wei Lai verfasserin aut In Pediatrics and Neonatology Elsevier, 2017 56(2015), 2, Seite 129-131 (DE-627)573750971 (DE-600)2441821-3 18759572 nnns volume:56 year:2015 number:2 pages:129-131 https://doi.org/10.1016/j.pedneo.2013.03.004 kostenfrei https://doaj.org/article/cc78978685504501baa2c6f87141d22c kostenfrei http://www.sciencedirect.com/science/article/pii/S1875957213000399 kostenfrei https://doaj.org/toc/1875-9572 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2004 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 56 2015 2 129-131 |
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A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. |
abstractGer |
A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. |
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A preterm male neonate was diagnosed as having microvillus inclusion disease based on the characteristics of histological and ultrastructural findings. The peripheral blood sample also revealed MYO5B mutation. He had been on long-term parenteral nutrition. However, a bowel segment was seen in the baby's diaper during hospitalization when he was 5 months old. Serial abdominal ultrasound demonstrated progressive dissection of the bowel wall with detached mucosa in real-time. Small intestinal epithelia were seen on the histology of the detached bowel segment. He died 2 weeks after the episode; postmortem autopsy showed diffuse detachment of mucosa of small bowels without perforation. This is the first report of an infant with microvillus inclusion disease that presented with bowel “dissection”. Weakened adhesion and integrity of intestinal epithelial cells caused by MYO5B mutation was speculated to result in the dissection and detachment of the epithelia of the gastrointestinal tract. |
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