salicylic acid has been researched along with Orphan Diseases in 27 studies
Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).
Orphan Diseases: Rare diseases that have not been well studied.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We diagnosed aplasia cutis congenita, a rare disorder with a wide variation in clinical symptoms." | 1.72 | [A child with a bald spot on her scalp]. ( de Jong, N; Janse, I, 2022) |
| "Bullous aplasia cutis congenita (BACC) is a rare clinical subtype that has few documented reports in the literature." | 1.56 | Bullous aplasia cutis congenita: A rare presentation of a rare disease. ( Watchmaker, J; Watchmaker, L, 2020) |
| "CONCLUSIONS Myeloid sarcoma, also called granulocytic sarcoma, is an extramedullary tumor of immature myeloid cells, which very rarely presents in children with APL." | 1.48 | A Rare Case of Relapsed Pediatric Acute Promyelocytic Leukemia with Skin Involvement by Myeloid Sarcoma. ( Alves, MJRG; Araújo, NS; Batinga, AMCS; Bomfim, LN; Calheiros Leite, LA; da Silva, MR; de Sousa Rodrigues, CF; Dos Santos Júnior, CJ; Gomes, VMDS; Gusmão, AKFDS; Romão, CMDSB, 2018) |
| "Cranial fasciitis of childhood (CFC) is a very uncommon tumour of the scalp, which is almost exclusively observed in the first years of life." | 1.46 | Cranial fasciitis of childhood (CFC): an unusual clinical case of a rare disease. ( Poddighe, D; Zavras, N, 2017) |
| "Twenty-two cases of aplasia cutis congenita were included in this study: 21 on the scalp and one on the foot heel." | 1.40 | Aplasia cutis congenita: clinical management and a new classification system. ( Berezovsky, AB; Krieger, Y; Landau, D; Levy, A; Pagkalos, VA; Rosenberg, L; Shoham, Y; Silberstein, E; Silberstein, T, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (14.81) | 29.6817 |
| 2010's | 19 (70.37) | 24.3611 |
| 2020's | 4 (14.81) | 2.80 |
| Authors | Studies |
|---|---|
| Daroach, M | 1 |
| Dogra, S | 1 |
| Bhattacharjee, R | 1 |
| Tp, A | 1 |
| Smith, F | 1 |
| Mahajan, R | 1 |
| Karinja, SJ | 1 |
| Mulliken, JB | 1 |
| de Jong, N | 1 |
| Janse, I | 1 |
| Mercadante, F | 1 |
| Piro, E | 1 |
| Busè, M | 1 |
| Salzano, E | 1 |
| Ferrara, A | 1 |
| Serra, G | 1 |
| Passarello, C | 1 |
| Corsello, G | 1 |
| Piccione, M | 1 |
| do Amaral Silva, A | 2 |
| Schettini, A | 2 |
| Mesquita, L | 2 |
| Carvalho Maron, SM | 2 |
| Bandeira de Melo, P | 2 |
| Francesconi, F | 2 |
| Watchmaker, L | 1 |
| Watchmaker, J | 1 |
| Rohani, P | 1 |
| Ramirez, R | 1 |
| Maluf, H | 1 |
| Kelly, KJ | 1 |
| Zavras, N | 1 |
| Poddighe, D | 1 |
| Araújo, NS | 1 |
| Dos Santos Júnior, CJ | 1 |
| Gomes, VMDS | 1 |
| Calheiros Leite, LA | 1 |
| Bomfim, LN | 1 |
| Gusmão, AKFDS | 1 |
| Alves, MJRG | 1 |
| Romão, CMDSB | 1 |
| Batinga, AMCS | 1 |
| da Silva, MR | 1 |
| de Sousa Rodrigues, CF | 1 |
| Ambooken, B | 1 |
| Kesavan, A | 1 |
| Neelakandan, A | 1 |
| Mathew, A | 1 |
| Chan, C | 1 |
| Magro, CM | 1 |
| Pham, AK | 1 |
| LeBlanc, RE | 1 |
| Yan, S | 1 |
| Barton, DT | 2 |
| Pace, NC | 1 |
| Chapman, MS | 1 |
| Momtahen, S | 1 |
| Bradburn, KH | 1 |
| Elston, D | 1 |
| Murphey, AW | 1 |
| Patel, KG | 1 |
| Khan, AM | 1 |
| Munir, A | 1 |
| Raval, M | 1 |
| Mehdi, S | 1 |
| Kawai, H | 1 |
| Hamasaki, T | 1 |
| Imamura, J | 1 |
| Tomonori, N | 1 |
| Odashiro, T | 1 |
| Yamahata, H | 1 |
| Tokimura, H | 1 |
| Nomoto, M | 1 |
| Arita, K | 1 |
| Chow, W | 1 |
| Griffiths, M | 1 |
| Tiger, JB | 1 |
| Habeshian, KA | 1 |
| Brennick, JB | 1 |
| Silberstein, E | 1 |
| Pagkalos, VA | 1 |
| Landau, D | 1 |
| Berezovsky, AB | 1 |
| Krieger, Y | 1 |
| Shoham, Y | 1 |
| Levy, A | 1 |
| Rosenberg, L | 1 |
| Silberstein, T | 1 |
| Oza, VS | 1 |
| Schulman, JM | 1 |
| Mully, TW | 1 |
| Ortiz, S | 1 |
| Techasatian, L | 1 |
| Waraasawapati, S | 1 |
| Jetsrisuparb, C | 1 |
| Jetsrisuparb, A | 1 |
| Dela Cruz, FS | 1 |
| Diolaiti, D | 1 |
| Turk, AT | 1 |
| Rainey, AR | 1 |
| Ambesi-Impiombato, A | 1 |
| Andrews, SJ | 1 |
| Mansukhani, MM | 1 |
| Nagy, PL | 1 |
| Alvarez, MJ | 1 |
| Califano, A | 1 |
| Forouhar, F | 1 |
| Modzelewski, B | 1 |
| Mitchell, CM | 1 |
| Yamashiro, DJ | 1 |
| Marks, LJ | 1 |
| Glade Bender, JL | 1 |
| Kung, AL | 1 |
| Chokoeva, AA | 1 |
| Patterson, JW | 1 |
| Tchernev, G | 1 |
| Knopp, E | 1 |
| Diette, K | 1 |
| Ko, C | 1 |
| Lazova, R | 1 |
| Jahan-Tigh, RR | 1 |
| Alston, JL | 1 |
| Umphlett, M | 1 |
| Stepanova, A | 1 |
| Marsch, WC | 1 |
| Stadie, V | 1 |
| Larsen, F | 1 |
| Birchall, N | 1 |
| Kennedy, A | 1 |
| Perry, D | 1 |
| Battin, M | 1 |
6 reviews available for salicylic acid and Orphan Diseases
| Article | Year |
|---|---|
Pachyonychia congenita responding favorably to a combination of surgical and medical therapies.
Topics: Administration, Topical; Combined Modality Therapy; Female; Genetic Predisposition to Disease; Human | 2019 |
Spontaneous Hair Repigmentation in an 80-Year-Old Man: A Case of Melanoma-Associated Hair Repigmentation and Review of the Literature.
Topics: Aged, 80 and over; Biopsy, Needle; Hair Color; Hair Follicle; Humans; Hyperpigmentation; Immunohisto | 2019 |
Blastic plasmacytoid dendritic cell neoplasm in the background of myeloproliferative disorder and chronic lymphocytic leukaemia.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Biopsy; CD4-Positive T-Lymphocytes; CD56 Antig | 2019 |
Three cases of spontaneous superficial temporal artery aneurysm with literature review.
Topics: Aged; Cerebral Angiography; Comorbidity; Female; Humans; Imaging, Three-Dimensional; Intracranial An | 2014 |
Giant Subcutaneous Solitary Gardner Fibroma of the Head of a Bulgarian Child.
Topics: Biopsy, Needle; Bulgaria; Child; Fibroma; Follow-Up Studies; Gardner Syndrome; Head; Humans; Immunoh | 2017 |
Basal cell carcinoma with metastasis to the lung in an African American man.
Topics: Aged; Biopsy, Needle; Black or African American; Carcinoma, Basal Cell; Combined Modality Therapy; F | 2010 |
21 other studies available for salicylic acid and Orphan Diseases
| Article | Year |
|---|---|
Scalp Nodules and Deformed Great Toes: Omens of Fibrodysplasia Ossificans Progressiva.
Topics: Hallux; Humans; Infant; Myositis Ossificans; Rare Diseases; Scalp | 2022 |
[A child with a bald spot on her scalp].
Topics: Alopecia; Ectodermal Dysplasia; Family; Female; Humans; Infant; Rare Diseases; Scalp | 2022 |
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene.
Topics: Humans; Noonan Syndrome; Rare Diseases; Scalp | 2022 |
Pink Lobulated Scalp Tumor: Answer.
Topics: Adult; Biopsy, Needle; Follow-Up Studies; Hair Diseases; Humans; Immunohistochemistry; Male; Pilomat | 2019 |
Bullous aplasia cutis congenita: A rare presentation of a rare disease.
Topics: Ectodermal Dysplasia; Female; Humans; Infant, Newborn; Rare Diseases; Scalp; Scalp Dermatoses | 2020 |
Longstanding microcystic adnexal carcinoma in a child.
Topics: Biopsy, Needle; Carcinoma, Skin Appendage; Child; Chronic Disease; Dermoscopy; Female; Follow-Up Stu | 2017 |
Cranial fasciitis of childhood (CFC): an unusual clinical case of a rare disease.
Topics: Child; Diagnosis, Differential; Fasciitis; Fibroblasts; Humans; Immunohistochemistry; Male; Rare Dis | 2017 |
A Rare Case of Relapsed Pediatric Acute Promyelocytic Leukemia with Skin Involvement by Myeloid Sarcoma.
Topics: Biopsy; Child; Fatal Outcome; Flow Cytometry; Humans; Leukemia, Promyelocytic, Acute; Male; Myeloid | 2018 |
Pink Lobulated Scalp Tumor: Challenge.
Topics: Adult; Biopsy, Needle; Diagnosis, Differential; Hair Diseases; Humans; Immunohistochemistry; Male; N | 2019 |
Pseudodidymosis: nevus psiloliparus with aplasia cutis congenita, an initial manifestation of Haberland syndrome.
Topics: Adipose Tissue; Alopecia; Child; Ectodermal Dysplasia; Eye Diseases; Genetic Pleiotropy; Humans; Lip | 2018 |
Trigeminal Trophic Syndrome-A Unique Clinical Presentation of a Rare Condition.
Topics: Female; Humans; Middle Aged; Rare Diseases; Scalp; Scalp Dermatoses; Skin Ulcer; Syndrome; Trigemina | 2019 |
A malignant eccrine spiradenoma of the scalp.
Topics: Adenoma, Sweat Gland; Adult; Biopsy, Needle; Eccrine Glands; Follow-Up Studies; Humans; Immunohistoc | 2014 |
Repigmentation of hair associated with melanoma in situ of scalp.
Topics: Aged, 80 and over; Biopsy, Needle; Carcinoma in Situ; Female; Hair Color; Hair Follicle; Humans; Imm | 2014 |
Aplasia cutis congenita: clinical management and a new classification system.
Topics: Ectodermal Dysplasia; Female; Follow-Up Studies; Graft Rejection; Graft Survival; Heel; Humans; Infa | 2014 |
A case of hair re-pigmentation from a scalp melanoma.
Topics: Biopsy, Needle; Diagnosis, Differential; Female; Hair; Hair Follicle; Humans; Hyperpigmentation; Imm | 2015 |
Hematidrosis: a report with histological and biochemical documents.
Topics: Acute Disease; Child; Hematologic Diseases; Hemorrhage; Humans; Male; Rare Diseases; Remission, Spon | 2016 |
A case study of an integrative genomic and experimental therapeutic approach for rare tumors: identification of vulnerabilities in a pediatric poorly differentiated carcinoma.
Topics: Adolescent; Animals; Antineoplastic Combined Chemotherapy Protocols; Carboplatin; Carcinoma; DNA Mut | 2016 |
Multiple blue macules and papules on the scalp.
Topics: Aged; Biopsy, Needle; Diagnosis, Differential; Female; Follow-Up Studies; Humans; Immunohistochemist | 2009 |
[A rare low-grade malignant scalp tumor. Atypical fibroxanthoma].
Topics: Aged; Head and Neck Neoplasms; Histiocytoma, Benign Fibrous; Humans; Male; Rare Diseases; Scalp; Sev | 2005 |
Cutis verticis gyrata: three cases with different aetiologies that demonstrate the classification system.
Topics: Adolescent; Adult; Diagnosis, Differential; Forehead; Humans; Infant, Newborn; Male; Rare Diseases; | 2007 |
Antenatal imaging of cutis verticis gyrata.
Topics: Cardiomyopathy, Hypertrophic; Diagnosis, Differential; Disease Progression; Fatal Outcome; Humans; I | 2008 |