A colonic mass revealing a disseminated crystal storing histiocytosis secondary to indolent multiple myeloma: a case report with literature review.


Journal

BMC gastroenterology
ISSN: 1471-230X
Titre abrégé: BMC Gastroenterol
Pays: England
ID NLM: 100968547

Informations de publication

Date de publication:
31 Jul 2020
Historique:
received: 19 12 2019
accepted: 02 07 2020
entrez: 2 8 2020
pubmed: 2 8 2020
medline: 15 5 2021
Statut: epublish

Résumé

Crystal storing histiocytosis is a rare disorder associated with monoclonal gammopathy. In this disease, monoclonal heavy and light chains accumulate in the lysosome of macrophages, leading to histiocytic reaction in different organs. It is secondary to the presence of a small B-cell clone, responsible for monoclonal immunoglobulin production. Histological diagnosis is a challenge and differential diagnoses include fibroblastic and histiocytic neoplasm. Clinical manifestations depend on the involved organs, rarely including peritoneum or digestive tract. We present a case of a 75-year-old with a medical history of colonic carcinoma. She presented with abdominal pain and inflammatory syndrome revealing a colonic mass. Hemicolectomy was performed. Initial diagnosis was fibroblastic tumour. The patient worsened, and diagnosis of a diffuse crystal storing histiocytosis was finally done. Haematological exploration found an indolent IgG-kappa multiple myeloma. The initial treatment with conventional chemotherapy did not permit an improvement of the patient condition. Immunotherapy with anti-CD38 monoclonal antibody (daratumumab) was proposed with a clinical and biological response. This case report emphasizes the histopathological challenge of histiocytic tumours which may involve digestive track. It focuses on the concept of monoclonal gammopathy of clinical significance, which can have a large spectrum of manifestations.

Sections du résumé

BACKGROUND BACKGROUND
Crystal storing histiocytosis is a rare disorder associated with monoclonal gammopathy. In this disease, monoclonal heavy and light chains accumulate in the lysosome of macrophages, leading to histiocytic reaction in different organs. It is secondary to the presence of a small B-cell clone, responsible for monoclonal immunoglobulin production. Histological diagnosis is a challenge and differential diagnoses include fibroblastic and histiocytic neoplasm. Clinical manifestations depend on the involved organs, rarely including peritoneum or digestive tract.
CASE PRESENTATION METHODS
We present a case of a 75-year-old with a medical history of colonic carcinoma. She presented with abdominal pain and inflammatory syndrome revealing a colonic mass. Hemicolectomy was performed. Initial diagnosis was fibroblastic tumour. The patient worsened, and diagnosis of a diffuse crystal storing histiocytosis was finally done. Haematological exploration found an indolent IgG-kappa multiple myeloma. The initial treatment with conventional chemotherapy did not permit an improvement of the patient condition. Immunotherapy with anti-CD38 monoclonal antibody (daratumumab) was proposed with a clinical and biological response.
CONCLUSION CONCLUSIONS
This case report emphasizes the histopathological challenge of histiocytic tumours which may involve digestive track. It focuses on the concept of monoclonal gammopathy of clinical significance, which can have a large spectrum of manifestations.

Identifiants

pubmed: 32736600
doi: 10.1186/s12876-020-01364-2
pii: 10.1186/s12876-020-01364-2
pmc: PMC7395414
doi:

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

239

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Auteurs

Adrien Contejean (A)

Haematology Department, AP-HP, Cochin University Hospital, 27 rue du Faubourg Saint Jacques, Paris, France.
Paris University, Paris, France.

Frédérique Larousserie (F)

Paris University, Paris, France.
Pathology Department, AP-HP, Cochin University Hospital, Paris, France.

Didier Bouscary (D)

Haematology Department, AP-HP, Cochin University Hospital, 27 rue du Faubourg Saint Jacques, Paris, France.
Paris University, Paris, France.

Anthony Dohan (A)

Paris University, Paris, France.
Radiology A Department, AP-HP, Cochin University Hospital, Paris, France.

Bénédicte Deau-Fischer (B)

Haematology Department, AP-HP, Cochin University Hospital, 27 rue du Faubourg Saint Jacques, Paris, France.

Tali-Anne Szwebel (TA)

Internal medicine Department, AP-HP, Cochin University Hospital, Paris, France.

Marion Dhooge (M)

Gastroenterology Department, AP-HP, Cochin University Hospital, Paris, France.

Benoit Terris (B)

Paris University, Paris, France.
Pathology Department, AP-HP, Cochin University Hospital, Paris, France.

Marguerite Vignon (M)

Haematology Department, AP-HP, Cochin University Hospital, 27 rue du Faubourg Saint Jacques, Paris, France. marguerite.vignon@aphp.fr.
Paris University, Paris, France. marguerite.vignon@aphp.fr.

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Classifications MeSH