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Characterization of circulating myeloma tumor cells by next generation flowcytometry in scleromyxedema patient: a case report.
Taha, Ruba Y; Hasan, Saba; Ibrahim, Firyal; Chantran, Yannick; Sabah, Hesham El; Sivaraman, Siveen; Bozom, Issam Al; Sabbagh, Ahmad Al; Garderet, Laurent; Omri, Halima El.
Afiliação
  • Taha RY; Hamad Medical Corporation, Hematology and Medical Oncology Department.
  • Hasan S; Hamad Medical Corporation, Hematology and Medical Oncology Department.
  • Ibrahim F; Hamad Medical Corporations, department and Laboratory Medicine and Pathology, Doha, Qatar.
  • Chantran Y; Department of Immunology, Hospital St Antoine, Paris, France.
  • Sabah HE; Hamad Medical Corporation, Hematology and Medical Oncology Department.
  • Sivaraman S; Hamad Medical Corporations, Interim Translational research Institute iTRI, Doha, Qatar.
  • Bozom IA; Hamad Medical Corporations, department and Laboratory Medicine and Pathology, Doha, Qatar.
  • Sabbagh AA; Hamad Medical Corporations, department and Laboratory Medicine and Pathology, Doha, Qatar.
  • Garderet L; Maladies du sang CHU de l'AP-HP Hôpital St-Antoine 184 rue du fg St-Antoine 75571 Paris, France.
  • Omri HE; Hamad Medical Corporation, Hematology and Medical Oncology Department.
Medicine (Baltimore) ; 99(27): e20726, 2020 Jul 02.
Article em En | MEDLINE | ID: mdl-32629647
ABSTRACT

INTRODUCTION:

Scleromyxedema (rare cutaneous mucinosis), is characterized by the formation of lichenoid papules and presence of Serum monoclonal IgG in most cases, or all; after repeated testing. PATIENT CONCERNS The patient is a 51-year-old male presented with thick, disfiguring elephant-like erythematous skin folds over the forehead, papular shiny eruptions over ears and trunk and waxy erythematous papules over arms and hands without dysphagia or respiratory or neurologic symptoms DIAGNOSIS Skin biopsy from right arm was consistent with scleromyxedema. Serum cryoglobulin was reported negative. Complete blood count and routine blood biochemistry were normal. Thyroid function tests were normal. Serum protein electrophoresis and immunofixation showed monoclonal band of 14.5 g/L typed as IgG lambda.

INTERVENTIONS:

Our patient was refractory to lenalidomide however improved clinically on immunoglobulins infusions on monthly basis without change in the MGUS level.

OUTCOMES:

NGF analysis revealed approximately 0.25% Lambda monotypic plasma cells in the bone marrow expressing CD38, CD138, and CD27 with aberrant expression of CD56 and were negative for CD45, CD19, CD117, and CD81. We also detected 0.002% circulating plasma cells (PCs) in peripheral blood.

CONCLUSION:

The immunophenotype of circulating tumor cells (CTCs) remain close to the malignant PCs phenotype in the BM. Hence, we report NGF approach as a novel diagnostic tool for highly sensitive MRD detection in plasma cell dyscrasias including scleromyxedema.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleromixedema / Citometria de Fluxo / Células Neoplásicas Circulantes Limite: Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleromixedema / Citometria de Fluxo / Células Neoplásicas Circulantes Limite: Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2020 Tipo de documento: Article