<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">IJCM</journal-id><journal-title-group><journal-title>International Journal of Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2158-284X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ijcm.2022.1311036</article-id><article-id pub-id-type="publisher-id">IJCM-120938</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Multiple Myeloma in a Patient with Rectal Cancer
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Huimin</surname><given-names>Fan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Caihua</surname><given-names>Tao</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Laboratory Medicine, Zhenjiang First People’s Hospital, Zhenjiang, China</addr-line></aff><pub-date pub-type="epub"><day>01</day><month>11</month><year>2022</year></pub-date><volume>13</volume><issue>11</issue><fpage>489</fpage><lpage>493</lpage><history><date date-type="received"><day>27,</day>	<month>September</month>	<year>2022</year></date><date date-type="rev-recd"><day>30,</day>	<month>October</month>	<year>2022</year>	</date><date date-type="accepted"><day>2,</day>	<month>November</month>	<year>2022</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Multiple myeloma is characterized by the accumulation of clonal, malignant plasma cells in the bone marrow. Multiple lytic skeletal lesions in some tumor patients with multiple myeloma are easily considered as bone metastases secondary to tumors, resulting in a missed diagnosis of multiple myeloma. Herein, we report a rare case, in which rectal cancer with multiple myeloma was initially misdiagnosed with bone metastases secondary to rectal cancer, due to the symptoms of multiple lytic sketetal lesions, and ignoring the abnormal plasma cells in the peripheral circulating blood smear. The patient was finally diagnosed with coexistence of rectal cancer and multiple myeloma. The case focuses on the importance of the peripheral circulating blood smear detection.
 
</p></abstract><kwd-group><kwd>Multiple Myeloma</kwd><kwd> Multiple Lytic Skeletal Lesions</kwd><kwd> Plasma Cell</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Multiple myeloma (MM) is the second most common hematologic malignancy [<xref ref-type="bibr" rid="scirp.120938-ref1">1</xref>] . It is mostly observed in older adults with a median age of 66 to 70 years [<xref ref-type="bibr" rid="scirp.120938-ref2">2</xref>] . MM is characterized by the accumulation of clonal, malignant plasma cells in the bone marrow [<xref ref-type="bibr" rid="scirp.120938-ref3">3</xref>] . It can affect many areas of the body, such as the bones, kidneys, eyes, and nerves [<xref ref-type="bibr" rid="scirp.120938-ref4">4</xref>] . In the majority of patients, malignant proliferation of plasma cells causes the M protein (abnormal IgG, IgM, or IgA or rarely IgE or IgD) in the serum and/or urine [<xref ref-type="bibr" rid="scirp.120938-ref5">5</xref>] . Multiple myeloma cells also produce abnormal light chain proteins (κ or λ). Therefore, the multiple myeloma process causes an excessive M protein level which leads to hyperviscosity [<xref ref-type="bibr" rid="scirp.120938-ref6">6</xref>] . Many symptoms of MM are vague. Patients may feel tired, unexplained weight loss, get frequent infections. Some patients even have no symptoms [<xref ref-type="bibr" rid="scirp.120938-ref7">7</xref>] . The uncontrolled growth of malignant plasma cells results in hypercalcemia, renal failure, anaemia, or destructive bone lesions (“CRAB”) [<xref ref-type="bibr" rid="scirp.120938-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.120938-ref9">9</xref>] . Pathological fractures may occur in the skull, spine, pelvis rib cage and the long bones. Many patients will often present with new bone pains or pathological fractures [<xref ref-type="bibr" rid="scirp.120938-ref10">10</xref>] . However, for some patients with tumors, bone is the most frequent site for metastasis [<xref ref-type="bibr" rid="scirp.120938-ref11">11</xref>] . These patients may present bone destruction. Therefore, multiple lytic skeletal lesions in some tumor patients with multiple myeloma are easily considered as bone metastases secondary to tumors, resulting in a missed diagnosis of MM. Herein, we report a case, in which rectal cancer with MM was initially misdiagnosed with bone metastases secondary to rectal cancer, due to the symptoms of multiple lytic sketetal lesions, and ignoring the importance of the peripheral circulating blood smear detection.</p></sec><sec id="s2"><title>2. Case Description</title><p>A 78-year-old man was diagnosed with rectal cancer at the local Hospital in 2017 and underwent radical surgery for rectal cancer, followed by postoperative chemotherapy for 6 rounds. He was referred to the respiratory department of our hospital due to fever and cough on July 15, 2021. CT showed multiple lytic skeletal lesions involving the spine, ribs and skull and vertebral compression fractures. Multiple postoperative bone metastases from the rectal cancer were diagnosed mainly involving the spine, ribs and skull. Routine blood specimens from this patient were tested in our laboratory. CBC showed a leukocyte count of 13.2 &#215; 10<sup>9</sup>/L (reference value: 3.5 &#215; 10<sup>9</sup>/L - 9.5 &#215; 10<sup>9</sup>/L), a hemoglobin concentration of 63 g/L (reference value: 130 g/L - 175 g/L) and a platelet count of 60 &#215; 10<sup>9</sup>/L (reference value: 125 &#215; 10<sup>9</sup>/L - 350 &#215; 10<sup>9</sup>/L). The peripheral blood smear showed plasma cells that contained round inclusions (Russell body), known as Motto cells (<xref ref-type="fig" rid="fig1">Figure 1</xref>). These changes are related to abnormal synthesis, trafficking or excretion of the immunoglobulin that is stored in excess within the cytoplasm [<xref ref-type="bibr" rid="scirp.120938-ref12">12</xref>] . Therefore, we suspected that the multiple lytic skeletal lesions were not bone metastases but were actually caused by multiple myeloma. Therefore, we continued to follow up on the other test results of this patient. Biochemistry showed total protein 131.60 g/L (reference value: 60 g/L - 80 g/L). Serum and urine electrophoresis demonstrated a monoclonal protein. Serum immunoglobulin showed IgG 135.00 g/L (reference value: 7.51 g/L - 15.6 g/L), IgA &lt; 0.0667 g/L (reference value: 0.82 g/L - 4.53 g/L), IgM &lt; 0.0417 g/L (reference value: 0.46 g/L - 3.04 g/L), β<sub>2</sub>-microglobulin 9.35 mg/L (reference value: 0 - 2.8 mg/L), serum free λ light chain 164.00 g/L (reference value: 3.13 g/L - 7.23 g/L), serum free κ light chain 0.22 g/L (reference value: 6.29 g/L - 13.5 g/L), urine free λ light chain 115.00 mg/L (reference value: 0 - 3.9 mg/L), and urine free κ light chain &lt; 6.940 mg/L (reference value: 0 - 7.1 mg/L). Multiple myeloma IgG-λ type was subsequently diagnosed.</p></sec><sec id="s3"><title>3. Discussion</title><p>MM is a type of haematological bone marrow malignancy. According to typical</p><p>symptoms and investigations, MM can be easily diagnosed for hematology specialists. However, for the non-specialist, MM or even coexistence of solid tumor and multiple myeloma is easily misdiagnosed or missed. Many patients with multiple myeloma initially present with bone pain involving long bones, rib skull, and pelvis. For many cancer patients, once cancer spreads to the bone, it is rarely cured and is associated with the symptoms including pain, increased risk of fracture, and hypercalcemia [<xref ref-type="bibr" rid="scirp.120938-ref13">13</xref>] . These symptoms are similar to the symptoms of MM. Therefore, multiple lytic skeletal lesions in some tumor patients with multiple myeloma are easily misdiagnosed with bone metastases secondary to tumors, resulting in a missed diagnosis of multiple myeloma. Herein, we report the case, in which rectal cancer with multiple myeloma was initially misdiagnosed with bone metastases secondary to rectal cancer, due to the symptoms of multiple lytic sketetal lesions, and ignoring the importance of the peripheral circulating blood smear detection. The abnormal plasma cells in the peripheral blood smear is a persuasive sign for a suspected diagnosis of MM. The presence of a high paraprotein and/or skewed imbalance of the κ/λ ratio is highly suggestive of diagnosis of MM.</p></sec><sec id="s4"><title>4. Conclusion</title><p>In clinical practice, some tumor patients with multiple myeloma are easily misdiagnosed with bone metastases secondary to tumors, resulting in a missed diagnosis of multiple myeloma. However, the coexistence of more than two kinds of tumors is not common, which can easily lead to clinical neglect. Therefore, we should pay attention to the hematological examination while performing the imaging examinations. The examination of peripheral blood smears is not only essential for diagnostics of hematological diseases but can also provide vital indications for the other diseases. By the systematic analysis of peripheral blood smears for alterations to blood cells, a blood smear test can make an important contribution to the formulation of a diagnosis [<xref ref-type="bibr" rid="scirp.120938-ref14">14</xref>] . Therefore, peripheral blood smears are an important screening method and should always be considered [<xref ref-type="bibr" rid="scirp.120938-ref15">15</xref>] .</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Fan, H.M. and Tao, C.H. (2022) Multiple Myeloma in a Patient with Rectal Cancer. International Journal of Clinical Medicine, 13, 489-493. https://doi.org/10.4236/ijcm.2022.1311036</p></sec></body><back><ref-list><title>References</title><ref id="scirp.120938-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Kazandjian, D. 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