Hirschsprung disease is a congenital anomaly characterised by an absence of innervation in the colon. The current diagnosis, which involves identifying the non-functional part of the colon through histological examination, is unsatisfactory. The objective of our study was to assess the potential of infrared spectroscopy as a label-free method to distinguish between functional and non-functional parts of the colon. Tissue samples from FFPE sections of Hirschsprung patients, taken from both functional and non-functional regions, were analysed by mid-infrared imaging. Colour-coded spectral images, reconstructed using multivariate data processing, were compared to the gold standard (hematoxylin-eosin-safran staining) to associate a specific spectral signature with each histological structure. Statistical analyses were also carried out to highlight infrared markers associated with Hirschsprung disease. The search for ganglion cells and cholinergic threads, the usual markers of the disease, was unsuccessful. However, our approach was efficient in differentiating between functional and non-functional parts of the colon by focussing on the muscularis. As such, vibrational spectroscopy can highlight biochemical differences that are not visible using standard histology. This proof-of-concept study suggests that vibrational spectroscopy is a candidate method for diagnosing Hirschsprung disease, paving the way for intraoperative application by assisting surgeons and histologists in delineating the pathological region.
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http://dx.doi.org/10.1039/d4an01489h | DOI Listing |
BMC Surg
March 2025
Faculty of Medicine, Catholic University of Bukavu, Bukavu, South Kivu, Democratic Republic of Congo.
Background: Hirschsprung disease (HD) contributes significantly to the burden of disease related to conditions amenable to pediatric surgery within the Democratic Republic of Congo (DRC). However, it has received less clinical attention due to limited resources. We aimed at assessing the long-term follow-up outcomes following an innovate resection approach in South Kivu, eastern DRC.
View Article and Find Full Text PDFArch Pathol Lab Med
March 2025
From the Departments of Laboratory Medicine and Pathology (Kapur) and Pediatric Surgery (Smith), Seattle Children's Hospital and University of Washington, Seattle.
Context.—: Surgery for Hirschsprung disease includes resection of the aganglionic bowel and adjacent transition zone (ganglionic bowel with partial circumferential aganglionosis, myenteric hypoganglionosis, and/or submucosal nerve hypertrophy). Pathology practices, including intraoperative frozen sections and sampling of resection specimens and accurate recognition and reporting of transition zone histopathology, are necessary to both prevent and diagnose incomplete resection.
View Article and Find Full Text PDFJ Pediatr Surg
March 2025
Department of Surgery, ANU Medical School, The Canberra Hospital, Garran ACT 2605, Australia. Electronic address:
The author comments on the recent paper by Cheng et al describing a series of MWS patients derived from a much larger series of HSCR patients. Children operated for HSCR with developmental delay suffer more difficulties than children without, but the literature varies on the outcomes associated with developmental delay such as Down syndrome and MWS. The author suggests that the degree of developmental delay has a bearing on outcome, and he further asks whether MWS has any particular features to make its prognosis different from other developmental delay syndromes associated with HSCR.
View Article and Find Full Text PDFFront Pediatr
February 2025
Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Department of Pediatric Surgery, Guangzhou Women and Children's Medical Center, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou Medical University, Guangzhou, Guangdong, China.
Introduction: Hirschsprung Disease (HSCR) is a common congenital intestinal disease in pediatrics. Early diagnosis and treatment after birth alleviate the occurrence of complications. Consequently, we aim to identifiy a biomarker with ease of use, non-invasiveness, and highly accurate for diagnosis.
View Article and Find Full Text PDFAnn Diagn Pathol
March 2025
Mashhad University of Medical Sciences, Department of Pathology, Mashhad, Iran. Electronic address:
Hirschsprung's disease (HSCR) is a congenital disorder of the intestine characterized by the absence of ganglion cells (GCs) in the myenteric and submucosal plexuses of the distal colon, leading to functional obstruction. The diagnosis of HSCR relies heavily on histopathological examination, yet pitfalls abound. Underdiagnosis can lead to delayed diagnosis, the need for reoperation, or risk of complications; conversely, overdiagnosis can lead to unnecessary surgery and its associated side effects.
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