Gastric Carcinoid in a Young Woman with Systemic Lupus Erythematosus and Atrophic Autoimmune Gastritis

Papadimitraki, Eva D.; Bree, Eelco de; Tzardi, Maria; Skordilis, Panagiotis; Kofteridis, Diamantis P.; Tsiftsis, Dimitris D.

doi:10.1080/00365520310001734

Cited by 16 publications

(15 citation statements)

References 15 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…Furthermore, the prevalence and the association of SLE and AIG itself are still unclear. The association of SLE and type I gastric carcinoid has rarely been reported previously (5,7,8). Although all three previously reported cases with type I gastric carcinoid with AIG and SLE showed pernicious anemia at the time of finding carcinoids (5, 7, 8), in the present case, vitamin B12 was low but pernicious anemia was not present when the carcinoid was detected, indicating that gastric carcinoid possibly occurred before the induction of pernicious anemia.…”

Section: Discussionmentioning

confidence: 38%

See 1 more Smart Citation

Successful Endoscopic Submucosal Dissection of Gastric Carcinoid in a Patient with Autoimmune Gastritis and Systemic Lupus Erythematosus

et al. 2012

View full text Add to dashboard Cite

A 41-year-old woman was referred with epigastric discomfort. She had a 20-year history of SLE. Esophagogastroduodenoscopy (EGD) examination showed severe atrophic gastritis in the stomach and a protruding lesion was detected. Histological examination showed a carcinoid tumor with cytoplasmic staining with chromogranin-A. Using an endoscopic submucosal dissection (ESD) technique, en bloc resection of the tumor was performed. No recurrence has been found for 3 years after the treatment. Type I gastric carcinoid can occur at an earlier age with AIG and autoimmune diseases such as systemic lupus erythematosus (SLE). This is the first report of gastric carcinoid that was treated by ESD.

show abstract

Section: Discussionmentioning

confidence: 38%

“…Therefore, the average age at detection of gastric carcinoids is in the 60s (3), and it rarely occurs at younger ages. In cases with other autoimmune disorders (4,5), type I gastric carcinoids may develop at a relatively young age. Pernicious anemia is usually already present when type I gastric carcinoid is detected.…”

Section: Discussionmentioning

confidence: 99%

Successful Endoscopic Submucosal Dissection of Gastric Carcinoid in a Patient with Autoimmune Gastritis and Systemic Lupus Erythematosus

et al. 2012

View full text Add to dashboard Cite

show abstract

“…A review of the literature revealed 14 cases of gastric cancer associated with SLE, consisting of 10 females and four males (aged 23‐72 years) . There were nine cases of adenocarcinoma, four cases of carcinoid tumor, and one case of neuroendocrine carcinoma of the stomach.…”

Section: Discussionmentioning

confidence: 99%

Systemic lupus erythematosus complicated with gastric cancer in an old man: A case report and literature review

Guo

Zhang

et al. 2018

Aging Medicine

View full text Add to dashboard Cite

“… ¶ Additional solid tumors have been reported in patients with systemic lupus erythematosus: biliary tract, 143 brain, 135,137,161 carcinoid (gastric), 171,172 colon, 133,135,137,140,142,143,152,153,161,173 connective tissue, 137 endocrine, 137 esophagus, 135,137 eye, 137 heart, 137 kidney, 133,135,137,139,142,152 lacrimal gland, 142 larynx, 135,137,161 melanoma, 135,137,143,174 oral, 135,137,142 pancreas, 133,135,137,139,142,152 rectum, 135,137,141 stomach, 135,137,142,143,153,161 testicles, 137,142 thyroid, 137,139,142,152,153,161 thymus, 175 urinary bladder, 135,137 and uterus 135,137,139,142,161 …”

Section: Systemic Lupus Erythematosusmentioning

confidence: 99%

Granuloma annulare, relapsing polychondritis, sarcoidosis, and systemic lupus erythematosus: conditions whose dermatologic manifestations may occur as hematologic malignancy‐associated mucocutaneous paraneoplastic syndromes

Cohen¹

2006

Int J Dermatology

View full text Add to dashboard Cite

IntroductionThe appearance of certain dermatoses has heralded either the diagnosis of a previously unsuspected malignancy or the detection of cancer recurrence in an oncology patient. 1,2 These associated mucosal and cutaneous conditions are referred to as mucocutaneous paraneoplastic syndromes. 3 In this issue, Zappasodi et al . 4 review some of the mucocutaneous paraneoplastic syndromes that occur in patients with hematologic malignancies. Albeit less commonly, other dermatologic conditions and systemic disorders can also occur in a paraneoplastic setting associated with hematologic malignancies: granuloma annulare, relapsing polychondritis, sarcoidosis, and systemic lupus erythematosus. Granuloma AnnulareGranuloma annulare is a chronic dermatosis of undetermined etiology. Clinically, the skin lesions present as flesh-colored to red papules and small nodules, which appear either as individual lesions or as an annular arrangement of confluent lesions. Mucin-containing areas of necrobiotic collagen in the dermis are surrounded by palisading granulomas consisting of epithelioid histiocytes, lymphocytes, and multinucleated giant cells.Granuloma annulare can be localized to a specific area of the body or generalized. Perforating and subcutaneous variants of the condition may also occur. Several factors have been described to precipitate the development of granuloma annulare: sunburn, drug eruption, flu-like illness, trauma, insect bites, and acute phlebitis. In addition, granuloma annulare has been observed in patients with potentially associated diseases -particularly diabetes mellitus and thyroid disease, but also drug allergy, hypertension, obesity, arthritis, atopy, sarcoidosis, and human immunodeficiency virus infection. [5][6][7][8][9] Skin lesions of leukemia or lymphoma that histopathologically mimic granuloma annulare have also been described in patients with hematologic malignancies. 10-14 Cancer-associated granuloma annulare has been reported predominantly in patients with hematologic malignancies (most commonly non-Hodgkin's lymphoma and Hodgkin's disease) and, less often, in individuals with solid tumors (Table 1). 5,6,[15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] Relapsing PolychondritisRelapsing polychondritis is a multisystemic disorder characterized by recurrent inflammation and degeneration of cartilaginous tissues -particularly those of the ears, nose, larynx, and trachea. [34][35][36][37] The dermatologic manifestations of relapsing polychondritis are variable and include aphthosis [oral and complex (genital)], nodules (on the extremities), purpura, papules, sterile pustules, superficial phlebitis, livedo reticularis, ulcers (on the extremities), and distal necrosis. 38 The aorta, bone, bronchi, central nervous system, ears, eyes, genitals, heart valves, kidneys, larynx, mouth, nose, and trachea are potential sites of extracutaneous involvement in patients with relapsing polychondritis. 34,38,39 The diagnostic criteria for relapsing polychondritis were initially e...

show abstract

Gastric Carcinoid in a Young Woman with Systemic Lupus Erythematosus and Atrophic Autoimmune Gastritis

Cited by 16 publications

References 15 publications

Successful Endoscopic Submucosal Dissection of Gastric Carcinoid in a Patient with Autoimmune Gastritis and Systemic Lupus Erythematosus

Successful Endoscopic Submucosal Dissection of Gastric Carcinoid in a Patient with Autoimmune Gastritis and Systemic Lupus Erythematosus

Systemic lupus erythematosus complicated with gastric cancer in an old man: A case report and literature review

Granuloma annulare, relapsing polychondritis, sarcoidosis, and systemic lupus erythematosus: conditions whose dermatologic manifestations may occur as hematologic malignancy‐associated mucocutaneous paraneoplastic syndromes

Contact Info

Product

Resources

About