Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 + 1479 word(s) 1479 2021-05-09 13:25:41 |
2 format change + 1 word(s) 1480 2021-05-28 06:22:26 | |
3 format change + 37 word(s) 1516 2021-05-28 06:24:42 | |
4 format change -1 word(s) 1515 2021-06-01 06:12:56 |

Video Upload Options

Do you have a full video?


Are you sure to Delete?
If you have any further questions, please contact Encyclopedia Editorial Office.
Reikvam, H. Crystal-storing Histiocytosis. Encyclopedia. Available online: (accessed on 25 June 2024).
Reikvam H. Crystal-storing Histiocytosis. Encyclopedia. Available at: Accessed June 25, 2024.
Reikvam, Håkon. "Crystal-storing Histiocytosis" Encyclopedia, (accessed June 25, 2024).
Reikvam, H. (2021, May 27). Crystal-storing Histiocytosis. In Encyclopedia.
Reikvam, Håkon. "Crystal-storing Histiocytosis." Encyclopedia. Web. 27 May, 2021.
Crystal-storing Histiocytosis

Crystal-storing histiocytosis (CSH) is a rare event in disorders associated with monoclonal gammopathy and is mostly associated with the accumulation of immunoglobulins (Igs) in the cytoplasm of histiocytes. 

Crystal-storing histiocytosis

1. Introduction

Crystal-storing histiocytosis (CSH) is a rare disorder characterized by the accumulation of crystallized deposits in the cytoplasm of histiocytes. The entity has been associated with underlying lymphoproliferative or plasma cell disorders, such as monoclonal gammopathy of undetermined significance (MGUS), multiple myeloma (MM), or lymphoplasmacytic lymphoma (LPL) [1][2][3]. The histiocytes in CSH contain crystallized material, although there have been reported cases of immunoglobulin-storing histiocytosis (IgSH) without a crystallized pattern of the deposited immunoglobulins [4][5]. IgSH can present in both a localized and a generalized form and may include a wide range of tissue sites and organs [1][2]. Herein, we present a patient with increasing back pain after a minor injury. She was diagnosed with a localized form of non-crystallized IgSH. We discuss the clinical findings, diagnostic workup, and therapeutic options. Furthermore, we performed a systematic review of the literature regarding IgSH and summarized the findings in this rare disease entity.

2. Case Report

A 75-year-old woman presented with acute pain in the lower back after a trivial incident. Her past medical history included hypertension, hypercholesterolemia, type 2 diabetes mellitus, hypothyroidism, migraine, and arrhythmia. Initial radiological examinations demonstrated no fracture. However, over the next few weeks, her back pain increased. By magnetic resonance imaging (MRI), she was diagnosed with a compression fracture in L1, although with no spinal stenosis (Figure 1). The fracture was initially managed conservatively; however, she had persistent opioid-dependent lower back pain and was admitted to the orthopedic department for further clinical and laboratory diagnostic workup to exclude a pathologic etiology for her fracture.
Figure 1. Magnetic resonance imaging (MRI) of lumbar column. The figure demonstrating collapse and fracture of vertebra corpus L1, with edema and compression against the spinal cord.
When blood tests revealed anemia, elevated sedimentation rate (SR), and a monoclonal (M)-protein by serum electrophoresis (Table 1), she was transferred to the hematology unit, as MM or other plasma cell dyscrasia was suspected. A bone marrow aspirate was performed and demonstrated a slightly hypocellular bone marrow with megakaryocytes present. There was normal maturation in the erythrocytopoiesis and the granulocytopoiesis, without expansion of lymphoid cells. The plasma cells accounted for 4% of nucleated marrow cells. Furthermore, whole-body low dose computed tomography (CT) for assessment of osteolytic lesion as part of MM was performed without detecting other lesions. Hence, the patient did not fulfill the diagnostic criteria for MM. However, based on the findings of monoclonal gammopathy by serum electrophoresis and the absence of findings supporting MM, she was diagnosed with MGUS. For further diagnostic workup, a CT-guided biopsy of the lesion in L1 was performed.
Table 1. Diagnostic blood test from the patients.
Analysis Values References
Hemoglobin (g/dL) 10.1 11.7–15.3
EVF 0.33 0.35–0.46
CRP (mg/L) 18 <5
SR (mm/t) 69 1–30
Creatinine (µmol/t) 78 45–90
Protein (g/L) 69 62–78
IgG (g/L) 16.1 6.0–15.3
IgA (g/L) 0.76 0.8–4.0
IgM (g/L) 0.51 0.3–2.30
Kappa free light chains (mg/L) 54.0 6.7–22.4
Lambda free light chains (mg/L) 25.0 8.3–27.0
Ratio kappa/lambda free light chains 2.16 0.31–1.56
S-protein electrophoresis Monoclonal band  
S-immunofixation Monoclonal band type IgG kappa.  
M-protein (mg/L) 7.1 0
The bone biopsy showed only sparse monoclonal plasma cells, but vast amounts of deposits intracellularly stored in histiocytes, inconsistent with amyloid (Figure 2). In immunohistochemical staining for light chains, the deposits were somewhat stronger positive for kappa than for lambda. In additional stains, IgG was colocalized with kappa and CD68, making it probable that the deposits consisted of whole immunoglobulins. By electron microscopic examination, there was abundant bright, predominantly amorphous material, but also some tubular structures with a diameter between 25–30 nm. No relation to cell organs was seen. Additionally, small amounts of electron-dense amorphous material were found. Attempts with mass spectrometry gave no conclusive results.
Figure 2. Histopathological examination of biopsy from corpus vertebrae. The figure demonstrates the biopsy from the patient’s corpus vertebrae L1. (A) Hematoxylin-eosin stain in low magnification demonstrating bone repair and bone marrow with the absence of organized hematopoiesis and maximal infiltration by histiocytes. (B) Hematoxylin-eosin stain in higher magnification demonstrating histiocytes with intracellular amorphous material. (C) Immunohistochemical staining for kappa light chain, demonstrating positivity in the histiocytes (brown color). (D) Electron microscopy, low magnification, showing bright intracellular material (left) and high magnification, showing no fibrils but spread tiny tubules (right).
After clinical, radiological, histopathological, and biochemical examination, it was concluded that the patient had MGUS with secondary IgSH, without any other underlying malignant disease. The patient had no sure sign of CRAB-criteria associated with MM: hypercalcemia, renal failure, anemia with Hb < 10 g/dL, or osteolytic bone disease. The patient, on the other hand, had persistent pain and difficulty moving, and she was, therefore, accepted for surgical intervention with vertebroplasty. She was operated on with the insertion of pedicle screws in vertebra corpora Th12 and L2, followed by repositioning of the fracture in L1 and the insertion of cement in the corpora with access via the pedicles bilaterally. The peri- and postoperative courses were without complications. The patient had striking relief of pain after surgery; she was no longer dependent on analgesics and could resume normal daily life activities. The current follow-up by the back surgeon and hematologist for her MGUS does not show signs of disease progression.

3. Literature Review

3.1. Methods and Classification

We performed a systematic PubMed search with the term “Storing Histiocytosis” in the title and identified 107 relevant published articles from 1987 to July 2020. The term “Storing Histiocytosis” was used to include both CSH and IgSH. Only cases with sufficient information written in English were included, and six articles were thereby rejected. From 101 articles, we identified 140 cases of assumed IgSH (Table 2). Other data collected were the type of material deposited within histiocytes, age, gender, involved sites, type of immunoglobulin if available, and the presence or not of an underlying lymphoproliferative disease or plasma cell dyscrasia.

3.2. Classification and Etiology

The median age at diagnosis was 60.5 years for both sexes (age-range women 18–91, age-range men 32–86), and there was a nearly equal sex distribution with 71 men (51%) and 69 women (49%) (Table 2). The age and gender distribution are presented in Figure 3. Cases were divided into two subgroups: localized and generalized, as proposed by Dogan et al. in 2012 [6]. Cases with only one involved site were characterized as localized (77%), while cases with two or more involved sites were classified as generalized (23%) (Table 2).
Figure 3. Age and gender distribution. The figure displays the incidence of storing histiocytosis in different decades. The median age at diagnosis was 60.5 years for both sexes (range 18–91, and slightly more cases were identified amongst men with 71 men (51%), compared to 69 women (49%).
Table 2. Demographic and pathological data from identified cases.
  Number (n) Percentage (%)
Men 71 51
Women 69 49
Localized 108 77
Generalized 32 23
1. SH with underlying LP–PCD 122 87
MM 43 31
LPL 21 15
MALT lymphoma 10 7
B-cell lymphoma not specified 2 1
2. SH without underlying LP–PCD 17 12
3. SH with unknown history 1 1

3.3. Organ Affection

IgSH can be found in a wide range of organs/tissues. The most frequently involved organ systems and tissue sites included bone, head and neck, kidney, lung, gastrointestinal mucosa, and lymph node. The organ and tissue site involvement in the identified cases is presented in Figure 4.
Figure 4. Affected organ systems. The figure demonstrates the number of identified cases in different organ systems. Abdomen unspecified includes one case of ascites and one case of a retroperitoneal mass. Abbreviations: GI—Gastrointestinal tract.

3.4. Immunoglobulin Classes and Immunoglobulin Restriction

Immunoglobulin classes were collected in this literature review and are presented in Figure 5. The information regarding the specific immunoglobulin and light chain present in the serum was not always available or specified. The most common immunoglobulin found by serum protein electrophoresis and immunofixation was IgG identified in 39 cases, while IgM and IgA were identified in 20 and 12 cases, respectively. The presence of light chains only was identified in nine cases (Figure 5). Hence, in most cases, the monoclonal spike was made of both heavy and light chains.
Figure 5. Prevalence of different immunoglobulins in Storing Histiocytosis. This figure demonstrates the distribution of immunoglobulin found in the serum by protein electrophoresis or immunofixation. Abbreviation: NA—not available.
The type of light chain, i.e., either kappa or lambda light chains, is presented in Figure 6. Kappa light chain was the most common light chain associated with IgSH (65 cases), either as part of complete Ig or as free light chain alone (Figure 6). Lambda light chain was only found in 10 cases.
Figure 6. Distribution of light chains. This figure demonstrates the distribution of light chains found in the serum by protein electrophoresis or immunofixation. Abbreviation: NA—Not available.

3.5. Etiology of Material Deposited

To include both non-crystallized and crystallized material within histiocytes, the term Storing Histiocytosis was used in the literature search. Three cases, including our present case, were described as “non-crystallizing” by histopathological review. On immunohistochemical analysis, the crystals are normally monoclonal, with eight exceptions in this review (Table 2). In many articles, information regarding the etiology of the crystals was insufficient and thereby classified as not available (NA). 6% had negative immunohistochemical staining for immunoglobulin, but many had an associated neoplastic B-cell disorder and had positive staining of plasma cells and lymphocytes in the surrounding area of the histiocytes and were described as an immunoglobulin-type of CSH.


  1. Flanagan, M.E.; Keene, C.D.; Louis, D.N.; Juric-Sekhar, G. Localized crystal-storing histiocytosis of the posterior fossa. Neuropathology 2018, 38, 529–534.
  2. Fang, H.; Chiu, A.; Reichard, K.K. Crystal-Storing Histiocytosis in Bone Marrow: A Clinicopathologic Study of Eight Cases and Review of the Literature. Am. J. Clin. Pathol. 2018, 149, 148–163.
  3. Lebeau, A.; Zeindl-Eberhart, E.; Muller, E.C.; Muller-Hocker, J.; Jungblut, P.R.; Emmerich, B.; Lohrs, U. Generalized crystal-storing histiocytosis associated with monoclonal gammopathy: Molecular analysis of a disorder with rapid clinical course and review of the literature. Blood 2002, 100, 1817–1827.
  4. Chantranuwat, C. Noncrystallized form of immunoglobulin-storing histiocytosis as a cause of chronic lung infiltration in multiple myeloma. Ann. Diagn. Pathol 2007, 11, 220–222.
  5. Kurabayashi, A.; Iguchi, M.; Matsumoto, M.; Hiroi, M.; Kume, M.; Furihata, M. Thymic mucosa-associated lymphoid tissue lymphoma with immunoglobulin-storing histiocytosis in Sjogren’s syndrome. Pathol. Int. 2010, 60, 125–130.
  6. Dogan, S.; Barnes, L.; Cruz-Vetrano, W.P. Crystal-storing histiocytosis: Report of a case, review of the literature (80 cases) and a proposed classification. Head Neck Pathol. 2012, 6, 111–120.
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to :
View Times: 434
Revisions: 4 times (View History)
Update Date: 01 Jun 2021
Video Production Service