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Institute of Clinical and Functional Anatomy

Univ.-Prof. Dr.med.univ. Marko Konschake
Univ.-Prof. Dr.med.univ. Marko Konschake
Institute of Clinical and Functional Anatomy

Müllerstraße 59
6020 Innsbruck

Phone: +43 (0)512 9003 71111
Fax: +43 (0)512 9003 71112
Email: Marko.Konschake@i-med.ac.at
Website: https://www.i-med.ac.at/Anatomie/

Research Branch (ÖSTAT Classification)

301102, 301103, 301104, 301106, 301107, 301111, 301112, 301113

Keywords

anatomical collection, Clinical-applied anatomy, digitalisation, human development, immunohistochemistry, lymphology, neuromonitoring, peripheral nerves, pre-/postgraduate education, and ultrasound

Research Focus

Our Institute has two major research topics: clinically applied anatomy and human development. We are applying classical anatomical methods in combination with modern imaging tools and operative and biomechanical methods. Human development is an important mainstay for descriptive and modern clinical and functional anatomy. We are microscopically examining various human adult and embryonic samples.           

General Facts

The major tasks of our Institute are research and education in human anatomy and embryology. The aim of anatomy is to understand the normal structures and architecture of the organism, while embryology aims to understand its normal development. Our research and education rely on an extensive body donation programme. We offer numerous lectures and pre- and postgraduate courses in anatomy for MDs, medical students, PhD students and physicians of various medical disciplines. We have seven research groups, all of which follow a translational, clinically applied approach, with an emphasis on peripheral nerves, human development, imaging, lymphology, skeletal development/ELMI, education and digitization and anatomical collection. We are applying a range of anatomical techniques in collaboration with national and international universities and university hospitals.

The graphic illustrates our scientific working groups (and personal team workflow):

Research

AGs Peripheral Nerves/Surgical Anatomy/ATCI and Imaging/Sonography (Konschake,Moriggl)

Our “Applied Anatomy” research is creating new minimally invasive surgical techniques, enhancing modern imaging methods and developing new clinical applications, particularly in neuro-sonography, using body donors and volunteers to ensure immediate implementation in patient care. The research is relevant to areas such as interventional radiology, (plastic) surgery and ENT, as well as to regional anaesthesia and pain management.

Common complications following low anterior resections include urinary and faecal incontinence and sexual dysfunction, often linked to damage of the pelvic autonomic nerves during surgery. To help surgeons protect these nerves, we have explored a new method for intraoperative pelvic neuromonitoring that relies on impedance measurements of the innervated organs. We have developed an algorithm (named AMINA) to classify bioimpedance signals. Thirty patients participated in a clinical trial involving nerve-preserving robotic rectal surgery with intraoperative pelvic neuromonitoring. The contraction of the urinary bladder and/or rectum, induced by direct stimulation of the nerves, led to a change in tissue impedance signals. We calculated features of the impedance signal and classified them to form AMINA, which automates the interpretation of impedance signals during intraoperative pelvic neuromonitoring. (Fig.1.)

Pelvic neuromonitoring principle based on direct nerve stimulation with a hand probe and
bioimpedance measurement of the bladder and rectum with a bipolar electrode montage. Contraction of the bladder and rectum smooth muscle in response to direct stimulation of the innervating autonomic nerves results in a change in the muscle tissue impedance. Assessment of stimulation-induced changes in tissue impedance allows the surgeon to identify and preserve the nerves. © Scientific Reports

Another example of our translational approach is “carpal tunnel release”, a common procedure with a high success rate but with the risk of iatrogenic injuries. We have explored the anatomy of the carpal tunnel, focusing on the proximity of neurovascular structures prone to injury, particularly during minimally invasive procedures. We noted the anatomical positions of the median nerve, ulnar nerve, ulnar artery and Berrettini branch in the carpal tunnels of 104 wrists from 52 body donors. We identified four major anatomical risk situations: (1) a proximal division of the middle-finger/ring-finger branch of the median nerve with a narrow safe zone; (2) an ulnar take-off of the recurrent muscle branch of the median nerve close to the distal ulnar end of the carpal tunnel; (3) an ulnar artery arch near the transverse carpal ligament; and (4) a proximal Berrettini branch close to this ligament. These anatomical features may place some patients at a higher risk of neurovascular injuries during minimally invasive carpal tunnel releases. We recommend a preoperative ultrasound assessment of at-risk neurovascular structures for those undergoing endoscopic or ultrasound-guided tunnel release. In high-risk patients, open surgery may be the safer option.

AG Human Development (Pechriggl)

VasKo: Vascular senescence as a key factor for cochlear health

Age-related hearing loss (ARHL) affects approximately one third of people over 65 worldwide. Both neuronal and vascular factors have a crucial role in its pathophysiology. We are investigating the impact of vascular senescence on cochlear health and developing new therapeutic approaches. We believe that age-related changes in cochlear blood supply impair the function of spiral ganglion neurons and thereby limit the success of cochlear implants (CI) in elderly patients. Improving cochlear blood flow by electrical stimulation (ES) or local pharmacological intervention could preserve neuronal vitality and optimize CI performance. This therapeutic approach requires a thorough assessment of age-related vascular alterations in the cochlea. We are characterizing the vascular microarchitecture of post-mortem human cochleae of 30 body donors by micro-CT and histological techniques. We are also examining the internal carotid artery to assess vascular health.

The project is being performed in cooperation with Med-El. It will provide the first systematic mapping of the cochlear vasculature in the geriatric population and will identify potential therapeutic targets. In the long term, we may even be able to modulate cochlear blood flow by implanted electrodes.

Infiltration of the blood vessels system with standard resins after embedding in Technovit 7100 resin (a-d). In the human modiolus we see good infiltration with the resin in most sections (a-c). The stria vascularis is not ideally preserved in this inner ear (d-arrows). Archival sections (e-g) with excellent preservation will complement our data with stereological evaluation. © MUI – Institute of Clinical and Functional Anatomy

AG Lymphology – Phlebology (Brenner)

Our major accomplishment was the publication of the book ‘Angewandte Lymphologie’ (together with Manuel E. Cornely and Wolfgang C. Marsch) in 2023 (Cornely et al., 2023; Figure 1); an English edition is due in 2025. Several papers have dealt with so-called lipoedema (Brenner, 2023; Brenner et al., 2023): we showed that body mass index is not a valid measure for the diagnosis of lipoedema and should be replaced by waist-to-height ratio. We also created a new S2k guideline on this clinical picture (Faerber et al., 2024; Figure 2). We have worked on the effectiveness of manual lymphatic drainage in breast cancer-related lymphedema (Kasseroller and Brenner, 2023) and Erich Brenner is involved in the development of an S3 guideline on the diagnosis and treatment of lymphoedema (AWMF Reg. No. 058-001), which is funded by the GBA Innovation Fund.

The hierarchical architecture of colour-producing tissue in ribbontail stingray. In blue regions of the skin, the chromatophore layer sandwiched between the collagen mat (CM) and lower dermis (loD) (A) consists of densely arranged iridophores (IP) and melanophores (M) grouped in chromatophore units and separated by vertical collagen bundles (vCF). Each chromatophore unit (B) involves a single melanophore (M) and multiple iridophores (IP), enfolding the black pigment melanophore with their numerous finger-like extensions. Note how the section plane intersects portions of all three iridophores (C). In slices through individual iridophores (D), they are seen to be densely packed with iridosomes (IS), the cellular organelles such as the nucleus (Nu) and Golgi apparatus (GA), mitochondria (Mi) and rough endoplasmic reticulum (rER) consolidated to the cell’s central body. The boxed area is depicted at higher magnification in (E). Iridosomes (IS) contain crystal platelets (Cr) and are kept in relative position by a dense scaffold of intermediate filaments (IF). © Blumer M.

AG Skeletal Development/ELMI (Blumer)

Structural colouration in nature

In animals, pigments and nanostructures determine skin colouration. We recently discovered a new mechanism for generating the blue colouration in the ribbontail stingray Taeniura lymma, a species with electric blue spots on its yellow-brown skin. We characterized fine-scaled differences in cell composition and architecture that distinguish blue from non-blue regions. In blue regions, the upper dermis comprises a layer of chromatophore units, iridophores and melanophores entwined in compact clusters framed by collagen bundles. Stingray iridophores differ from other vertebrate light-reflecting cells in having numerous finger-like processes that surround nearby melanophores like fists clenching a black stone. Iridophores contain spherical iridosomes that enclose guanine nanocrystals, suspended in a 3D quasi-order, linked by a cytoskeleton of intermediate filaments. We argue that intermediate filaments form a structural scaffold with a distinct optical role, providing the iridosome spacing critical to produce the blue colour. In contrast, black-pigmented melanosomes within melanophores show space-efficient packing, consistent with their hypothesized role as broadband absorbers for enhancing the blue colour. In non-blue areas, iridophores are replaced by pale cells, resembling iridophores in some morphological and nanoscale features but lacking guanine crystals. The cellular associations and structural interactions in stingray skin suggest that pigment cells induce differentiation in the progenitor cells of iridophores and that some features driving colour production may be shared with bony fishes, although the lineages diverged hundreds of millions of years ago and the iridophores themselves differ drastically. (Fig. 3)

Pictures

Selected Publications

Kaiser P, Schmidle G, Bode S, Seeher U, Honis HR, Moriggl B, Pechriggl E, Stofferin H, Konschake M. Clinical-applied anatomy of the carpal tunnel regarding mini-invasive carpal tunnel release. Arch Orthop Trauma Surg. 2024 Nov;144(11):4753-4765.  https://doi.org/10.1007/s00402-024-05560-7

Schuler R, Langer A, Marquardt C, Kalev G, Meisinger M, Bandura J, Schiedeck T, Goos M, Vette A, Konschake M. Automatic muscle impedance and nerve analyzer (AMINA) as a novel approach for classifying bioimpedance signals in intraoperative pelvic neuromonitoring. Sci Rep. 2024 Jan 5;14(1):654. https://doi.org/10.1038/s41598-023-50504-7

Brenner, E., Forner-Cordero, I., Faerber, G., Rapprich, S., Cornely, M., 2023. Body mass index vs. waist-to-height-ratio in patients with lipohyperplasia dolorosa (vulgo lipedema). J Dtsch Dermatol Ges 21:1179-1185. http://dx.doi.org/10.1111/ddg.15182.

Surapaneni, V.A., Blumer, M.J., Tadayon, K., McIvor, A.J., Redl, S., Hornis, H.-R., Mollen, F.H., Amini, S., Dean, M.N. (2024). Ribbontail Stingray Skin Employs a Core–Shell Photonic Glass Ultrastructure to Make Blue Structural Color. Adv. Optical Mater. https://doi.org/10.1002/adom.202301909

Selection of Funding

  1. FFG Bridge Grant: KFA-Medel
  2. FEI Grant: KFA-EyeCre-Addion “Forschung Entwicklung Innovation” Land Tirol, F.47167/9-2023
  3. Educational Grants KFA-Medel

Collaborations

Prof.Dr. José Sanudo, MD, Prof.in Dr.in Teresa Vazquez, MD, Complutense University of Madrid, Center of Body Donation, Madrid, Spain

Prof.Dr. Jeffrey Janis, MD, FACS, Department of Plastic Surgery, Ohio State University Medical Center in Columbus, Ohio, USA

Univ.Prof.Dr. Fabrice Duparc, Université de Rouen, Rouen, France

Prof.Dr. David Chen, MD, FACS, Lichtenstein Amid Hernia Clinic at UCLA Section of Minimally Invasive Surgery, UCLA Division of General Surgery, Los Angeles, USA

Univ.-Prof. Thomas Fichtner-Bendtsen, MD, Ass.-Prof. Jens Børglum Neimann, MD, Department of Clinical Medicine Anesthesiology, Copenhagen, Denmark

Univ.-Prof. Vincent Chan, MD, University Health Network – Toronto Western Hospital, Toronto, Canada

Department of Infectious Diseases & Public Health Jockey Club College of Veterinary Medicine and Life Sciences City University of Hong Kong, Department of Biomaterials Max Planck Institute of Colloids and Interfaces (Germany).