reticulohistiocytosis

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re·tic·u·lo·sis

(re-tik'yū-lō'sis),

An increase in histiocytes, monocytes, or other reticuloendothelial elements.

[reticulo- + G. -osis, condition]

Farlex Partner Medical Dictionary © Farlex 2012

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References in periodicals archive ?

Our case had no features of multicentric reticulohistiocytosis or fibroblastic rheumatism.

Erosive Arthritis, Fibromatosis, and Keloids: A Rare Dermatoarthropathy

Based on the clinical features and aforesaid investigations, the differential diagnoses of nodular/histoid leprosy, reticulohistiocytosis, subcutaneous sarcoidosis, cutaneous localised leishmaniasis, lymphocytoma cutis, mycosis fungoides and post kala azar dermal Leishmaniasis were considered.

Lymph node abscess and cardiac involvement in a patient with nodular lepromatous leprosy (LL) with erythema nodosum leprosum (ENL): a rare occurrence

Roentgenologic features of osteoarthritis, erosive osteoarthritis, ankylosing spondylitis, psoriatic arthritis, Reiter's disease, multicentric reticulohistiocytosis, and progressive systemic sclerosis.

A study of enthesitis in Spondyloarthropathy in patients from a tertiary care service hospital

This process encompasses several disorders of variable extent and severity, historically known as histiocytosis X, Letterer-Siwe disease, Hand-Schuller-Christian syndrome, eosinophilic granuloma of bone, and self-healing reticulohistiocytosis. (63) In the last few years, the debate whether LCH is a reactive or neoplastic process has been re-energized by the discovery that LCH is a clonal process.

Nonneoplastic lesions that simulate primary tumors of bone

Multicentric reticulohistiocytosis is a rare systemic disease presenting with subcutaneous nodular lesions and symmetrical, erosive polyarthritis.

Multicentric reticulohistiocytosis and cancer: a case report and review of the literature.

Paraneoplastic rheumatic disorders / Paraneoplastik romatizmal hastaliklar

An unusual form of histiocytosis, namely congenital self-healing reticulohistiocytosis (CSHRH or Hashimoto-Pritzker disease) generally follows a benign clinical course and its incidence may be underestimated due to a high rate of spontaneous resolution and lack of clinical recognition.

An infant with recurrent maculopapular rashes, anemia, lymphadenopathy, and hepatosplenomegaly

Solitary congenital self-healing reticulohistiocytosis in monozygotic twins.

Congenital self-healing reticulohistiocytosis (Hashimoto-Pritzker disease): case report/ Kendiliginden duzelen dogumsal retikulohistiyositoz (Hashimoto-Pritzker hastaligi): olgu sunumu

IPGME&R, Kolkata Diagnosis Ulcerative multicentric reticulohistiocytosis.

PhotoDermDiagnosis - Swelling of small joints and multiple ulcers near metacarpophalangeal joints

There are several case reports in literature where leprosy has been confused with other diseases, common mimicrs being sarcoidosis, (6) cutaneous lymphomas, (7,8) Jessner's lymphocytic infiltrate, (9) multicentric reticulohistiocytosis, (10) and connective tissue diseases.

Type II reaction without erythema nodosum leprosum masquerading as lymphoma

(7) Notable exceptions are solitary and multicentric reticulohistiocytosis, which are usually negative for factor XIIIa.

Cutaneous Rosai-Dorfman disease with increased number of eosinophils: coincidence or histologic variant?