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<article xml:lang="EN" article-type="case-report">

<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Blood Res</journal-id>
<journal-id journal-id-type="publisher-id">BR</journal-id>
<journal-title-group>
<journal-title>Blood Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">2287-979X</issn>
<issn pub-type="epub">2288-0011</issn>
<publisher>
<publisher-name>Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis</publisher-name>
</publisher>
</journal-meta>

<article-meta>
<article-id pub-id-type="doi">10.5045/br.2019.54.4.241</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Images of Hematology</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Chronic lymphocytic leukemia with unusual cytoplasmic anomalies</article-title>
</title-group>

<contrib-group>

<contrib contrib-type="author" corresp="yes">
<name>
<surname>Athanase</surname>
<given-names>Nicolas</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

</contrib-group>

<aff id="A1">Laboratoire d'h&#x00E9;matologie, Centre Hospitalier Agen-N&#x00E9;rac, Agen, <country>France</country>.</aff>

<author-notes>
<corresp>Correspondence to Nicolas Athanase, M.D., Laboratoire de Biologie M&#x00E9;dicale, Centre Hospitalier Agen-N&#x00E9;rac, Route de Villeneuve sur Lot, Saint-Esprit 47923 Agen, France, <email>athanase.nicolas@gmail.com</email>, <email>athanasen@ch-agen-nerac.fr</email></corresp>
</author-notes>

<pub-date pub-type="ppub">
<month>12</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>20</day>
<month>12</month>
<year>2019</year>
</pub-date>
<volume>54</volume>
<issue>4</issue>
<fpage>241</fpage>
<lpage>241</lpage>

<history>
<date date-type="received">
<day>21</day>
<month>08</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>10</day>
<month>09</month>
<year>2019</year>
</date>
</history>

<permissions>
<copyright-statement>&#x00A9; 2019 Korean Society of Hematology</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder>Korean Society of Hematology</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0">
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://creativecommons.org/licenses/by-nc/4.0">http://creativecommons.org/licenses/by-nc/4.0</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
</article-meta>
</front>

<body>

  <p><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="br-54-241-g001"></graphic></p>
  <p>An 82-year-old woman was admitted for cardiac insufficiency associated with obesity, renal insufficiency, and refractory atrial fibrillation. The patient had no history of hematological malignancies. Clinical examination revealed no lymphadenopathy, tumoral syndrome, or weight loss. Hematological tests showed the following: platelets, 173&#x00D7;10<sup>9</sup>/L; hemoglobin, 10.3 g/dL; white blood cells, 10.5&#x00D7;10<sup>9</sup>/L; and lymphocytes, 5.60&#x00D7;10<sup>9</sup>/L. Cytological examination of blood smear indicated the presence of small lymphocytes with very mature chromatin, regular nuclei, and multiple intracytoplasmic sharp vacuoles, accounting for 41% of the total lymphocytes, as determined by manual differential white blood cell count (Panel <bold>A&#x2013;I</bold>, May-Gr&#x00FC;nwald Giemsa Staining; &#x00D7;1,000). Flow cytometry analysis indicated the typical profile of chronic lymphocytic leukemia (CD5&#x002B;, CD23&#x002B;, FMC7&#x2212;, CD22&#x2212;, CD43&#x002B;, and low monoclonal lambda chain). Due to the advanced age of the patient, cytogenetic analysis was not performed. Vacuoles are spherical organelles consisting of a double lipid layer; they contain intra or extracellular proteinaceous material.</p>
  <p>Vacuoles in lymphocytes have been reported in lysosomal storage diseases and neoplastic disorders; moreover, they are physiologically present in T and natural killer lymphocytes. Although vacuoles are more or less specific, they deserve attention as they can offer valuable insights.</p>

</body>

</article>