Sinus histiocytosis with massive lymphadenopathy: Complicated by autoimmune hemolytic anemia

Penukonda, Sasi; Sowdi, Vasantha; Shetty, Sumanth Bellipady; Venugopal, U.; Parameshwariah, S.; Dias, Edwin; Kamala, C. S.

doi:10.1007/bf02724322

Cited by 3 publications

(2 citation statements)

References 5 publications

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“…It may be explained by the association of autoimmune haemolytic anaemia (AIHA) which was also reported by earlier workers [3,6]. AIHA has been well reported in malignant lymphoma.…”

Section: Discussionsupporting

confidence: 57%

Sinus Histiocytosis with Massive Lymphadenopathy – Its Rare Immunological Complication

Ghosh¹

2015

J Cancer Sci Ther

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A 3-year-old boy presented with irregular fever, multiple painless swelling over neck, axilla and inguinal region for one and half year. The child developed progressive pallor for one to two months. Examination revealed generalized lymphadenopathy including massive cervical lymphadenopathy, hepatosplenomegaly, severe anaemia and absence of jaundice. Here, a case of sinus histiocytosis with massive lymphadenopathy complicated by a rare immune dysregulation in the form of autoimmune haemolytic anaemia is reported.

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“…It may be explained by the association of autoimmune haemolytic anaemia (AIHA) which was also reported by earlier workers [3,6]. AIHA has been well reported in malignant lymphoma.…”

Section: Discussionsupporting

confidence: 57%

Sinus Histiocytosis with Massive Lymphadenopathy – Its Rare Immunological Complication

Ghosh¹

2015

J Cancer Sci Ther

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“…Acute life-threatening autoimmune hemolytic anemia has been described in several reports [ 8 , 9 , 10 ]. However, only 4 pediatric patients [ 11 , 12 , 13 ], including our case, with significant acute autoimmune hemolytic anemia, have been identified (Table 1 ). All patients had lymphadenopathy and symptoms of anemia upon presentation, along with low hemoglobin, high reticulocytes, and a strong positive direct antiglobulin test.…”

Section: Discussionmentioning

confidence: 99%

Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature

et al. 2018

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Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided.

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Abdominal tuberculosis with autoimmune hemolytic anemia

Gupta

2005

Indian J Pediatr

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An eight-year-old male child presented with progressive distension of abdomen, fever, pallor and jaundice with a history of tubercular contact. Investigations were suggestive of abdominal tuberculosis with autoimmune hemolytic anemia. The child responded well to a course of oral steroids with antitubercular treatment. A literature search did not reveal any previous case report of an association between tuberculosis and autoimmune hemolytic anemia.

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Sinus histiocytosis with massive lymphadenopathy: Complicated by autoimmune hemolytic anemia

Cited by 3 publications

References 5 publications

Sinus Histiocytosis with Massive Lymphadenopathy – Its Rare Immunological Complication

Sinus Histiocytosis with Massive Lymphadenopathy – Its Rare Immunological Complication

Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature

Abdominal tuberculosis with autoimmune hemolytic anemia

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