Lupus is a systemic autoimmune disease with a broad spectrum of clinical presentations evolving by flare-ups and remissions [1] [2]. It is more common on young females. Estimated incidence rates in USA and Europe range 1 - 23 per 100,000 per year. Prevalence in adults is as high as 150 per 100,000 in United States and is 20 - 50 per 100,000 in Europe [3] [4]. Its etiology is unclear but many observations suggest a role of genetic and environmental factors such as immunologic, hormonal factors, physical factors. It has variable mode of onset ruled by cutaneous, articular and hematological disorders [3] [4]. Other uncommon and life-threatening manifestations can reveal the disease such as hemorrhagic features. There are several reports of hemorrhagic features. Li J. et al. reported 8% of hemorrhagic cases in their study [5]. We report 6 cases of lupic disease disclosed by a hemorrhagic syndrome.

It’s about a retrospective, descriptive and multicentric study range from 1st January 2014 to 5th January 2019. Were included in the study all cases of lupic disease revealed by hemorrhagic disorders, recorded in 3 Internal Medicine Departments in Dakar: DalalJamm, Dantec, Pikine. The diagnosis of lupus was made on the basis of the 1997 modified classification criteria of ACR. If the patients had at least 4 criteria on 11 then they were classified as a Lupus. The data analysis was made with Microsoft excel 2007 and SPSS version 20.

We gathered 6 cases of women affected by lupic disease. The mean age was 32 years old with extremes range 17 and 56 years. According to hemorrhagic disorders, the diagnosis of lupus was automatically made in 5 of the cases and it took 6 months to confirm the last one. Hemorrhagic features were ruled by purpura (3 cases) and nosebleeding associated to gumbleeding (2 cases) (Table 1). Cutaneous (5/6) and articular (4/6) disorders specially represented the other manifestations. Biological findings showed cytopenia with 3 cases of anaemia, 1 case of leucopenia and 6 cases of thrombopenia (Table 2).

The average of the platelet count was at 20,000 cells/mm³ with extremes range from 1000 to 35,000 cells/mm³. Thrombocytopenia was related to autoimmune thrombocytopenic purpura in 3 cases, to Evans syndrome in 2 cases, to macrophage activation syndrome in 1 case (Figure 1). Immunological investigations found the presence of antinuclear antibodies in 1 patient, anti-dsDNA in 2 patients and anti-Sm in 4 patients (Table 2). All the patients received a bolus of Solumedrol followed by an administration of Prednisone at a dosage of 1.5 mg/kg (3 cases) and 1 mg/kg to the other patients. A transfusion of platelet concentrates was performed for all of them. They were under Azathioprine and Hydroxychloroquine respectively at a dosage of 100 mg/day and 400 mg/day, after having a normal platelet count. The evolution was favorable in 4 cases. Two patients died according to a septic and haemorrhagic shock.

We conducted a study on inaugural hemorrhagic manifestations that lead to the diagnosis of lupic disease.

Articular, cutaneous and hematologic features are the leading modes of onset of lupic disease [3] [4]. Hematologic disorders of the lupus are common at early stage or at the time of diagnosis. Up to date, hemorrhagic onset is rare as we can note with the rarity of medical reports in our level [6] [7] [8]. Li J and coll noted

hemorrhagic disorders during lupus at a frequency of 8% while Jallouli and coll found a frequency of 6% [5] [9]. In 2010 in Senegal, Fatou Samba and coll reported 2 cases of hemorrhagic manifestations that to say 1.4% in her series [10]. We report 6 cases of hemorrhagic manifestations revealing the lupic disease.

The occurrence of hemorrhagic manifestations during lupic disease is a diagnostic and therapeutic emergency, as we could see in our study where we had 5 patients on whom the diagnosis of lupic disease was made during hospitalization.

Lupic disease is a condition that mostly occurs in women at their thirthies [3] [4]. This inequality is due to hormonal factors involvement especially œstrogens by a stimulation of the immune system. Hemorrhagic manifestations are not excepted as shown in many studies [5] [9] [11]. In our study, the mean age was estimated at 32 years with extremes range 17 and 56 years old. Li and coll found in their study in regard to thrombocytopenia during lupus with hemorrhagic features, an average age of 34.8 ± 14.6 years proving the early onset of the condition and its hallmarks [5].

In our study, purpura, epistaxis and gingivorragia constituted the main hemorrhagic manifestations. These data are similar to those reported on the literature [5] [6] [11]. Li J. and coll found that 70% of bleeding patients with severe thrombocytopenia (<20,000 platelets/mm³) and 75% with moderate thrombocytopenia had cutaneo-mucous involvement. According to that, how severe the thrombocytopenia could be, the predilection of hemorrhage would be cutaneo-mucous.

At the time of diagnosis, the main manifestations were articular and cutaneous. That was similar to the findings according to the literature where the manifestations occur simultaneously to the initial clinical course [5] [9] [11].

The thrombocytopenia occurring during lupic disease is due to a lack of production of the bone marrow, a splenic sequestration or a rapid peripheral destruction related to the autoimmune process. Commonly, that’s a mild low platelet count [12]. Hemorrhagic features mostly occur with moderate (20.000 - 50.000 cells/mm³) to severe (less than 20.000 cells/mm³) thrombocytopenia [5] [9] [11]. Li J. and coll found that 76% of people with severe low platelet count underwent a hemorrhage against 25% patients with moderate low platelet count [5]. This leads to say the lower the platelet count is, the higher the risk of bleeding. In Tunisia, Jallouli and coll found similar datas [9]. This is proven in our study with a mean platelet count of 20.000 cells/mm³ with extremes range of 1000 and 50,000 cells/mm³.

These low platelet levels were mostly associated with idiopathic autoimmune thrombocytopenia, antiphospholipid syndrome, Evans’ syndrome. Autoimmune thrombocytopenia related to lupus is defined by a platelet count less than 100.000 cells/mm³ without another underlying cause. It occurs in 7% - 30% cases of lupus. Antiphospholipid syndrome is a condition featuring thrombotic manifestations, obstetrical accidents and antiphospholipid antibodies. Evans syndrome is characterized by the association of autoimmune haemolytic anaemia and thrombocytopenia [12]. An association of thrombocytopenia with Evans syndrome was found in 12.5% by Tokano and coll, in 1.2% by Li and coll and 18% by Ziakas and coll [5] [11] [13]. Li and coll found an association of thrombocytopenia with antiphospholipid syndrome in 6% of cases while Jallouli and coll found 14.3% cases. In our study, thrombocytopenia was associated with autoimmune thrombopenic purpura in 50% of cases, in 33% with an Evans syndrome and 17% with macrophage activation syndrome. The different findings could be explained by a selection bias in our study. Because all our patients presented haemorrhagic manifestations with thrombocytopenia. However, the studies were conducted on people having thrombocytopenia with or without haemorrhagic manifestations.

The diagnosis of lupic disease is confirmed on the basis of biological and immunological findings especially the dosage of fluorescent antinuclear antibodies. Further investigations can be performed for more specific antibodies such as anti-dsDNA and anti-Sm. The series provided by Jallouli and coll showed a positivity of anti-dsDNA antibodies in 73.5% and anti-Sm in 32.4% respectively. The one conducted by Jung and coll showed a positivity of 100% of anti-DNA and 8.3% of anti-Sm on patients with thrombocytopenia. Ziakas and coll reported, respectively, a positivity of 100% for antinuclear antibodies, 56% for anti-DNA and 10% for anti-Sm [9] [11] [14]. In our series, the presence of antinuclear antibodies were noted in 17% of the cases, while anti-DNA and anti-Sm were respectively found in 33% and 60% of the cases. The different findings could be explained by the ethnical and racial difference in our studied populations. In fact, Meyer and coll noticed a sensibility of anti-Sm antibodies of 30% on African Americans and 3% to 7% in european series. Anti-Sm sensibility is especially high on black people with a proportion of 50% compared to what is seen in Caucasians on whom we note a proportion of 10% to 20% of SLE cases [15].

The urgent management of autoimmune thrombocytopenia or secondary haemorrhagic manifestations during lupus requires high doses of glucocorticoids. A second-line treatment may consist on the administration of immunosuppressors such as azathioprine and cyclophosphamide. In case the aforementioned molecules don’t work, rituximab can be used as a third-line treatment. Transfusion of concentrates platelets should be performed only if the platelet count is less than 10.000 cells/mm³ [12]. In our study, the patients received a bolus of methylprednisolone followed by prednisone at a dosage of 1.5 mg/kg and 1 mg/kg. After normalizing the platelet count, patients were under azathioprine at a dosage of 100 mg/day and hydroxychloroquine at a dosage of 400 mg/day. All patients underwent a transfusion of concentrates platelets.

After treatment, the evolution was favorable in 4 patients. Two patients died after due to haemorrhagic and septic shock. This was similar to the datas reported on the literature. Central neurological disorders and infections constitute the leading mortality causes after inaugural haemorrhage. Li J and coll reported a mortality rate of 12.1% on bleeding patients. They also found a mortality rate estimated at 13% on patients with mild to severe thrombocytopenia as a leading cause. Infections and hemorrhagic shock respectively caused 49% and 33% of deaths [5] [9] [11] [14]. This points out the importance of an early diagnosis and management of these manifestations.

The limitation of our study is the small sample of our study. That is not enough to take real statement and tendency on clinical and paraclinical findings that appeared with an initial hemorrhagic manifestation that lead to the lupus’ diagnosis.

We report 6 cases of Lupus revealed by hemorrhagic disorders. Mostly, the bleeding areas are cutaneous and mucous associated with mild to severe thrombocytopenia related to autoimmune thrombocytopenic purpura. They occur with the presence of anti-Sm antibodies. A study conducted on a larger sample would be necessary, on black African people, to point out the prevalence of hemorrhagic manifestations during systemic lupus and its pathogenesis.

The authors declare no conflicts of interest regarding the publication of this paper.

Codou, F.B., Dimitri, W., Mouhamed, D., Bamba, D., Johanita, T., Ahmadou, G., Aly, S., Cheikh, N.A., Fall, C.A., Maimouna, S., Ndour, M.A., Boundia, D., Sy, K.B., Seynabou, F., Abdoulaye, L., Abdoulaye, P. and Souhaibou, N. (2021) Haemorrhagic Lupus: A Diagnosis Emergency, Report about 6 Cases. Open Journal of Internal Medicine, 11, 231-237. https://doi.org/10.4236/ojim.2021.114019