Results 21 to 30 of about 1,204 (194)

LINFOMA LINFOPLASMACÍTICO SECRETOR DE IGG/KAPPA EVOLUINDO COM ANEMIA HEMOLÍTICA E INSUFICIÊNCIA RENAL

Hematology, Transfusion and Cell Therapy, 2021
Relato de caso: Paciente, sexo feminino, 43 anos, sem comorbidades, admitida na clínica cirúrgica do Hospital Jean Bitar (HJB) devido quadro de massa abdominal hipogástrica.
BLSA Lima, YA Medeiros, EA Fonseca, LFSK Pantoja, MA Pinto, VS Sirqueira, JS Fujishima, JRM Barros, JCP Saraiva-Filho, TX Carneiro   +9 more
doaj   +1 more source

Necrobiotic xanthogranuloma associated with smoldering multiple myeloma: satisfactory response to cyclophosphamide, dexamethasone, and thalidomide [PDF]

Anais Brasileiros de Dermatologia, 2019
: Necrobiotic xanthogranuloma is a rare chronic condition, belonging to the group C non-Langerhans cell histiocytoses, which is relevant due to the possibility of extracutaneous involvement and association with systemic diseases, particularly hematologic
Renan Bernardes de Mello, Everton Carlos Siviero do Vale   +1 more
doaj   +1 more source

Xantoma plano difuso normolipêmico idiopático com hiperesplenismo Diffuse plane idiopathic normolipemic xanthoma with hiperesplenism

Anais Brasileiros de Dermatologia, 2010
O xantoma plano difuso normolipêmico é doença rara, do grupo das histiocitoses, caracterizada pelo aparecimento de placas amareladas ou amarelo-alaranjadas, distribuídas simetricamente na pele e geralmente acompanhadas por xantelasma.
Danielle Machado da Silva, Jorge João Chacha, Nayara de Castro Wiziack, Luiz Carlos Takita, Fernando Kenzo Hayashi   +4 more
doaj   +1 more source

Are African primary physicians suspicious enough? Challenges of multiple myeloma diagnosis in Africa

The Egyptian Journal of Internal Medicine, 2021
Background Multiple myeloma is a hematological malignancy of plasma cells belonging to a spectrum of monoclonal protein-secreting disorders known as paraproteinemias.
Erick Thokerunga, Christopher Ntege, Abdullahi Omar Ahmed   +2 more
doaj   +1 more source

Diffuse plane xanthomatosis associated with monoclonal gammopathy Xantomatose plana difusa associada a gamopatia monoclonal

Anais Brasileiros de Dermatologia, 2011
Diffuse plane normolipemic xanthomatosis (DPNX) is a rare, non-inherited disease that is often associated with systemic diseases, mainly malignant hematological (especially multiple myeloma) or lymph proliferative disorders.
Aristóteles Rosmaninho, Iolanda Fernandes, Arlindo Guimas, Isabel Amorim, Manuela Selores   +4 more
doaj   +1 more source

Recurrence of membranoproliferative glomerulonephritis post transplant – Is this mere recurrence of pattern or recurrence of disease?

Saudi Journal of Kidney Diseases and Transplantation, 2019
Recurrence of membranoproliferative glomerulonephritis (MPGN) is seen in 1965% cases of postrenal transplant resulting in graft loss in up to 35-50% of cases.
Umesh Lingaraj, Shivanagouda Ramanagouda Patil, Kishan Aralapuram, Shivaprasad Sasivehalli Mallappa, Sreedhara Chikkanayakanahalli Gurusiddaiah, Mahesha Vankalakunti   +5 more
doaj   +1 more source

Scleromyxedema without paraproteinemia

International Journal of Dermatology, 2014
AbstractBackgroundScleromyxedema is a rare generalized form of lichen myxedematosus, a chronic cutaneous mucinosis of unknown etiology usually associated with a monoclonal gammopathy and underlying systemic disorders. It is characterized by the presence of lichenoid papules and diffuse indurations of the skin.
Abarzúa, Alvaro A., Giesen, Laura F., Sandoval, Mauricio O., González, Sergio B.   +3 more
openaire   +3 more sources

Xantogranuloma necrobiótico solitário sem paraproteinemia Necrobiotic xanthogranuloma without paraproteinemia

Anais Brasileiros de Dermatologia, 2008
O xantogranuloma necrobiótico é doença crônica granulomatosa e xantomatosa, caracterizada por pápulas e placas infiltradas, eritematosas e amareladas, preferencialmente localizadas na região periorbital.
Danielle Mazziero Macedo, Sérgio Henrique Hirata, Nílceo S. Michalany, Mílvia Maria Simões, Silva Enokihara, Mauro Y. Enokihara   +5 more
doaj   +1 more source

Clinical observation of monoclonal fibrillary glomerulonephritis

Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
Monoclonal gammopathy of renal significance is a condition caused by the proliferation of a clone of B-lymphocytes or plasma cells that does not reach the criteria required for the initiation of treatment for oncohematological indications, but is ...
T. A. Garkusha, F. V. Alyab'ev, T. A. Vdovik   +2 more
doaj   +1 more source

Subcorneal Pustular Dermatosis, a Systematic Review and Pooled Analysis of a Rare and Underdiagnosed Disease

JEADV Clinical Practice, EarlyView.
ABSTRACT Background Subcorneal pustular dermatosis (SPD), or Sneddon–Wilkinson disease, is a rare, relapsing pustular skin condition of unknown cause, characterised by subcorneal pustules. Objectives To summarise the demographic, clinical, histopathological, management and disease course of SPD.
Mason H. Crossman, Jeffrey Weng, Alysha Vuong, Lawrence Lin, Zhao Feng Liu, Christopher Y. Chew   +5 more
wiley   +1 more source