<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Normoblasts on Leukoformula</title><link>https://www.leukoformula.com/en/tags/normoblasty/</link><description>Recent content in Normoblasts on Leukoformula</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Tue, 02 Jun 2026 09:00:00 +0300</lastBuildDate><atom:link href="https://www.leukoformula.com/en/tags/normoblasty/feed.xml" rel="self" type="application/rss+xml"/><item><title>Howell-Jolly Bodies &amp; Binucleated Normoblasts in Blood Smear</title><link>https://www.leukoformula.com/en/post/telca-zholli-i-dvuhyadernye-normoblasty-v-mazke-40441/</link><pubDate>Tue, 02 Jun 2026 09:00:00 +0300</pubDate><guid>https://www.leukoformula.com/en/post/telca-zholli-i-dvuhyadernye-normoblasty-v-mazke-40441/</guid><description>&lt;p>Newborn infant.&lt;/p>
&lt;p>Peripheral blood. Erythrocyte with a Howell-Jolly body (photo 1) and a binucleated normoblast with a Howell-Jolly body (photo 2).&lt;/p>
&lt;p>🙏 The publication was kindly provided by &lt;a href="https://vk.com/id17266368" target="_blank" rel="noopener nofollow ugc">Ekaterina Nozdrina&lt;span class="link-ext" aria-hidden="true">↗&lt;/span>&lt;/a>, Omsk.&lt;/p></description></item><item><title>Bone Marrow Erythroid Lineage in Multiple Myeloma</title><link>https://www.leukoformula.com/en/post/eritroidnyy-rostok-kostnogo-mozga-pri-mielomnoy-39813/</link><pubDate>Mon, 11 May 2026 08:00:00 +0300</pubDate><guid>https://www.leukoformula.com/en/post/eritroidnyy-rostok-kostnogo-mozga-pri-mielomnoy-39813/</guid><description>&lt;p>Patient, 71 years old, diagnosed with multiple myeloma.&lt;/p>
&lt;p>Complete blood count:&lt;/p>
&lt;p>RBC 3.6×10^12/L&lt;/p>
&lt;p>HGB 128 g/L&lt;/p>
&lt;p>WBC 4.0 g/L&lt;/p>
&lt;p>PLT 210×10^9/L&lt;/p>
&lt;p>ESR 18 mm/hour.&lt;/p>
&lt;p>In the control bone marrow aspirate, after a course of treatment, the erythroid lineage of hematopoiesis is expanded to 47.5% (normal range 14.5-26.5). Binucleated erythrokaryocytes (photo 2, 3) and mitotic figures (photo 5) are observed.&lt;/p></description></item><item><title>Bone Marrow Erythroid Hyperplasia in Splenomegaly Case</title><link>https://www.leukoformula.com/en/post/giperplaziya-eritroidnogo-rostka-kostnogo-mozga-39258/</link><pubDate>Sat, 25 Apr 2026 08:00:00 +0300</pubDate><guid>https://www.leukoformula.com/en/post/giperplaziya-eritroidnogo-rostka-kostnogo-mozga-39258/</guid><description>&lt;p>SPLENOMEGALY in a 56-year-old PATIENT.
Complete blood count without abnormalities:
RBC 4.66×10&lt;sup>12/L
HGB 142 g/L
WBC 3.43×10&lt;/sup>9/L
PLT 149 ×10^9/L.&lt;/p>
&lt;p>In the bone marrow aspirate, the granulocytic lineage is relatively narrowed (35.4%), lymphocytes are 13.5% (normal 4.3-13.7%), and erythrocaryocyte proliferation is significantly increased (45.0%). Binucleated erythrocaryocytes are observed. Megakaryocytes show preserved functional capacity.&lt;/p></description></item><item><title>Proerythroblast: Morphological Features of the Cell</title><link>https://www.leukoformula.com/en/post/proeritroblast-morfologicheskie-osobennosti-kletki-38303/</link><pubDate>Tue, 14 Apr 2026 08:00:00 +0300</pubDate><guid>https://www.leukoformula.com/en/post/proeritroblast-morfologicheskie-osobennosti-kletki-38303/</guid><description>&lt;p>PROERYTHROBLAST is a young, large cell of the erythroid lineage of hematopoiesis, with a round nucleus containing delicate reticular chromatin, a nucleolus, and intensely basophilic cytoplasm.&lt;/p>
&lt;p>🙏 The publication was kindly provided by KDL physician &lt;a href="https://vk.com/id850941842" target="_blank" rel="noopener nofollow ugc">Nana Novikova&lt;span class="link-ext" aria-hidden="true">↗&lt;/span>&lt;/a>, CHUZ &amp;ldquo;KB&amp;rdquo; RZHD-Meditsina&amp;quot;, Smolensk.&lt;/p></description></item><item><title>Blood Smear in Beta-Thalassemia Post-Splenectomy</title><link>https://www.leukoformula.com/en/post/mazok-krovi-pri-beta-talassemii-posle-splenektomii-37307/</link><pubDate>Thu, 19 Mar 2026 09:00:01 +0300</pubDate><guid>https://www.leukoformula.com/en/post/mazok-krovi-pri-beta-talassemii-posle-splenektomii-37307/</guid><description>&lt;p>👉🏻Severe anisopoikilocytosis in a patient with beta-thalassemia and splenectomy.&lt;/p>
&lt;p>➖This is a hereditary blood disorder in which the synthesis of beta-globin chains is impaired.&lt;/p>
&lt;p>🩸Peripheral blood&lt;/p>
&lt;p>🔹The smear contains target cells (codocytes) characteristic of thalassemia (photo 1)&lt;/p></description></item><item><title>Autoimmune Hemolytic Anemia: Blood Smear Morphology</title><link>https://www.leukoformula.com/en/post/autoimmunnaya-gemoliticheskaya-anemiya-36771/</link><pubDate>Wed, 25 Feb 2026 18:00:00 +0300</pubDate><guid>https://www.leukoformula.com/en/post/autoimmunnaya-gemoliticheskaya-anemiya-36771/</guid><description>&lt;p>Autoimmune hemolytic anemia caused by warm antibodies&lt;/p>
&lt;p>Polychromasia and spherocytes are found in the peripheral blood; circulating erythroblasts and occasional Howell-Jolly bodies may be present.&lt;/p>
&lt;p>The disease is caused by immunoglobulin G class antibodies that react with red blood cells at temperatures of 37 degrees Celsius and above. This is the most common form of autoimmune hemolytic anemia.&lt;/p></description></item></channel></rss>