Humberto Martinez-Cordero
Overview
Explore the profile of Humberto Martinez-Cordero including associated specialties, affiliations and a list of published articles.
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13
Citations
17
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Recent Articles
1.
Bolivar S, Medina P, Fuentes M, Martinez-Cordero H, Salguedo G
Cureus
. 2024 Oct;
16(9):e68674.
PMID: 39371703
A solitary extraosseous plasmacytoma is a rare type of plasma cell neoplasm. Its occurrence in the stomach is particularly unusual and can easily be mistaken for more common types of...
2.
Prieto-Torres A, Esparza-Albornoz A, Ovalle-Roa N, Pisciotti-Chajin I, Martinez-Cordero H
Cureus
. 2024 Sep;
16(8):e67386.
PMID: 39310528
Paraproteinemias or monoclonal gammopathies constitute a broad spectrum of heterogeneous clonal disorders of plasma cells characterized by the secretion of monoclonal proteins of heavy or light chains and the development...
3.
Martinez-Cordero H, Fuentes-Lacouture C, von Glasenapp A, Pena C
Curr Opin Oncol
. 2024 Sep;
36(6):610-614.
PMID: 39246175
Purpose Of Review: Health disparities or inequities, which are defined as differences in the quality of medical and healthcare between populations among racial, ethnic, and socioeconomic groups, have been validated...
4.
Hungria V, Pena C, Gomez-Almaguer D, Martinez-Cordero H, Schutz N, Blunk V
EJHaem
. 2024 Aug;
5(4):867-878.
PMID: 39157594
The incidence of multiple myeloma (MM) has surged globally, particularly in Latin American countries, and is attributable to an aging population and increased life expectancy. This systematic review analyzes the...
5.
Prieto-Torres A, Rojas-Torres A, Salguedo G, Martinez-Cordero H
Cureus
. 2024 Aug;
16(7):e64411.
PMID: 39130868
Hemophagocytic lymphohistiocytosis (HLH) is a rare but potentially life-threatening syndrome characterized by excessive immune activation and tissue inflammation. This case report describes the early diagnosis of HLH in an adult...
6.
Gallardo-Perez M, Negrete-Rodriguez P, Gertz M, Pena C, Riva E, Gilli V, et al.
Acta Haematol
. 2024 Aug;
:1-9.
PMID: 39128463
Introduction: POEMS syndrome is a rare paraneoplastic syndrome caused by an underlying plasma cell disorder. The acronym refers to the following features: polyradiculoneuropathy, organomegaly, endocrinopathy, monoclonal paraproteinemia, and skin changes....
7.
Ramirez-Gamero A, Martinez-Cordero H, Beltran B, Florindez J, Malpica L, Castillo J
Am J Hematol
. 2024 May;
99(8):1586-1594.
PMID: 38767403
Disease Overview: Plasmablastic lymphoma (PBL) is a rare CD20-negative aggressive lymphoma with a poor prognosis under standard treatment options. Though PBL is associated with human immunodeficiency virus infection and other...
8.
Martinez-Cordero H, Pena C, Schutz N, Bove V, Villano F, Beltran C, et al.
JCO Glob Oncol
. 2023 Dec;
9:e2300182.
PMID: 38060975
Purpose: Multiple myeloma (MM) is a highly heterogeneous, incurable disease most frequently diagnosed in the elderly. Therefore, data on clinical characteristics and outcomes in the very young population are scarce....
9.
Riva E, Hungria V, Chiattone C, Martinez-Cordero H
Hematol Oncol Clin North Am
. 2023 May;
37(4):801-807.
PMID: 37258356
Waldenström macroglobulinemia (WM) is a rare, indolent, and currently incurable B-cell neoplasm characterized by monoclonal immunoglobulin M gammopathy, frequent nodal involvement, and lymphoplasmacytic infiltration of the bone marrow. The clinical...
10.
Pena C, Riva E, Schutz N, Ramirez A, Vasquez J, Del Carpio D, et al.
Leuk Lymphoma
. 2023 Jan;
64(4):816-821.
PMID: 36695519
Primary plasma cell leukemia (pPCL) is an infrequent and aggressive plasma cell disorder. The prognosis is still very poor, and the optimal treatment remains to be established. A retrospective, multicentric,...