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      Microcirculatory pathways in normal human spleen, demonstrated by scanning electron microscopy of corrosion casts.

      1 , ,
      The American journal of anatomy
      Wiley

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          Abstract

          Confusion regarding microcirculatory pathways in normal human spleen has arisen due to extrapolation from pathological material and from other mammalian spleens, not to mention difficulties in tracing intricate three-dimensional routes from the study of thin sections or cut surfaces of tissue. We examined microcirculatory pathways in normal human spleens freshly obtained from organ transplant donors. A modified corrosion casting procedure was used to obtain an open view of vessels and their connections. Our results demonstrate: 1) "arteriolar-capillary bundles" within lymphatic nodules and extensive branching of arterioles in the marginal zone (MZ); 2) the marginal sinus around lymphatic nodules; 3) the peri-marginal cavernous sinus (PMCS) outside the MZ or immediately adjacent to the nodule itself; the PMCS receives flow via ellipsoid sheaths and MZ, or directly from arterial capillaries, and drains into venous sinuses; 4) fast pathways for flow into venous sinuses via ellipsoid sheaths; 5) arterial capillary terminations in the reticular meshwork of the red pulp or MZ ("open" circulation); direct connections to venous sinuses also occur ("closed" circulation), although rarely; and 6) numerous open-ended venous sinuses in the MZ, allowing a large proportion of the splenic inflow to bypass the red cell filtration sites in the reticular meshwork and at venous sinus walls.

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          Author and article information

          Journal
          Am J Anat
          The American journal of anatomy
          Wiley
          0002-9106
          0002-9106
          Mar 1988
          : 181
          : 3
          Affiliations
          [1 ] Department of Biophysics, University of Western Ontario, London, Canada.
          Article
          10.1002/aja.1001810304
          3364384
          c772bf98-9235-44b2-bca0-c2ba1342fd0b
          History

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